Patents
Literature
Hiro is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Hiro

35 results about "Methoxybenzoates" patented technology

3-Methoxybenzoic acid was used in the synthesis and characterization of 3-methoxybenzoates of europium (III) and gadolinium (III). It was used in conversion of aromatic carboxylic acids into methyl esters and reduction to the corresponding primary alcohols using a sodium borohydride-THF-methanol system.

Method for preparing N-(3,5-dichloropyridyl-4-yl)-3-cyclopropylmethoxy-4-difluoromethoxybenzoyl amine

The invention discloses a method for preparing N-(3,5-dichloropyridyl-4-yl)-3-cyclopropylmethoxy-4-difluoromethoxybenzoyl amine, which is implemented by carrying out amidation reaction on anions of 4-amino- -3,5-dichloropyridine and 3-cyclopropylmethoxy-4-difluoro-aryl-methoxybenzoate under inert solvent neutralized alkaline conditions. The preparation method disclosed by the invention has the advantages of mild reaction conditions, fewer byproducts and simple after-treatment, and obviously lowers the synthesis cost; the purity of the refined product is at least 99.8%; and the invention is more suitable for industrial large-scale production.
Owner:CHENGDU EASTON BIOPHARMACEUTICALS CO LTD

(+)-4-methoxybornyl benzoate and its preparation method and application

The present invention relates to a kind of bornyl benzoate and its preparation method and application, its chemical structure is shown in following formula (I), and chemical name is (+)-4-methoxybornyl benzoate. The synthetic method of bornyl benzoate of the present invention is that (+)-borneol, 0.75 times of borneol quality 4-methoxybenzoic acid, 0.025 times of borneol quality p-toluenesulfonic acid are added in toluene, It was obtained by reacting at 120°C for 8 hours. The (+)-4-methoxybornyl benzoate of the present invention has low cytotoxicity and the effect of penetrating the blood-brain barrier, and can promote medicines to penetrate the blood-brain barrier.
Owner:GUANGZHOU UNIVERSITY OF CHINESE MEDICINE

High-strength long-service-life titanium-silver backboard of household appliance

The invention relates to a high-strength long-service-life titanium-silver backboard of a household appliance. The high-strength long-service-life titanium-silver backboard is sequentially provided with a titanium-silver white refined coating, a joining layer, a titanium-silver white pre-coating, a first passivation layer, a galvanized plate, a second passivation layer and a titanium-silver white back coating, wherein the titanium-silver white refined coating comprises polyamide resin, silver powder, silver oxide, titanium dioxide and a surfactant; the titanium-silver white back coating comprises polyester resin, aluminum powder, zinc oxide, titanium dioxide and a surfactant; and the joining layer comprises a propyne-butyl acrylate copolymer, polyethylene glycol and octyl p-methoxybenzoate. Through improving the structure and formula of the coating of the backboard of the household appliance according to the scheme, not only is the favorable bending processability of the backboard not influenced, but also the backboard has the characteristics of acid and alkaline resistance, solvent resistance and ageing resistance and can still keep relatively high coating bonding strength if being in a humid environment or under a relatively large temperature difference condition for a long term, and the coating is good in substrate adhesive force, incapable of losing the luster, free of dust accumulation on the surface and free of pulverizing, cracking or blistering phenomenon if being used for a long term.
Owner:扬子江新型材料(苏州)有限公司

(+)-2-methoxybornyl benzoate and its preparation method and application

InactiveCN102267912AGood permeation of the blood-brain barrierOrganic active ingredientsNervous disorderBenzoic acidChemical structure
The present invention relates to a kind of bornyl benzoate and its preparation method and application, its chemical structure is shown in following formula (I), and chemical name is (+)-2-methoxybornyl benzoate. The synthetic method of bornyl benzoate of the present invention is that (+)-borneol, 0.75 times of borneol quality 4-methoxybenzoic acid, 0.025 times of borneol quality p-toluenesulfonic acid are added in toluene, It was obtained by reacting at 120°C for 8 hours. The (+)-2-methoxybornyl benzoate of the present invention has low cytotoxicity and the effect of penetrating the blood-brain barrier, and can promote medicines to penetrate the blood-brain barrier.
Owner:GUANGZHOU UNIVERSITY OF CHINESE MEDICINE

Zafirlukast intermediate preparation process

The invention relates to a zafirlukast intermediate preparation process, wherein the compound is an important intermediate for preparing a leukotriene antagonist drug zafirlukast. The process comprises: carrying out a heating reaction in an inert solvent under the action of acidified montmorillonite by using methyl(5-nitro-1-tosyl-1H-indole-3-yl)acetate and methyl 3-methoxybenzoate as raw materials until the raw materials disappear, filtering to obtain 3-methoxy-4-[(5-nitro-1-tosyl-1H-indole-3-yl)methyl] methyl benzoate, and hydrolyzing the 3-methoxy-4-[(5-nitro-1-tosyl-1H-indole-3-yl)methyl]methyl benzoate under alkaline conditions to obtain the target product. According to the present invention, the new process route for synthesizing the important zafirlukast intermediate is provided,has the technical advantages of simple operation, low reaction cost, high product yield and environmental friendliness, and can meet the large-scale production demand of medical products.
Owner:NANJING MEDICAL UNIV

Leonurine crystal and use thereof in preparation of insulin sensitizer, hypoglycemic drug and lipid-lowering drug

This invention belongs to the modern pharmaceutical field of Traditional Chinese Medicine, and relates to an herbal extract of Chinese Motherwort and its application in pharmacy, which specifically relates to the crystal structure of a Chinese Motherwort extract: Leonurine, and its application in the preparation of medicine. The chemical name of the above-mentioned Leonurine is 4-guanidino-1-)butyl 4-hydroxy-3,5-dimethoxybenzoate. The invention by specific methods prepares leonurine as 6 kinds of crystals with different crystal forms. Specifically, there are six different structures of leonurine sulfate crystals, two of them are hydrate, two are anhydrous crystal form, one is methanol solvate, one is ethanol solvate. The leonurine crystal forms of this invention can applicate in preparing medicine such as insulin sensitizer, hypoglycemic and lipid-lowering drugs. The above mentioned insulin sensitizers are particularly useful in treating insulin resistance syndrome, and the above mentioned lipid-lowering drugs are useful in the treatment of disorders of lipid metabolism, hyperlipidemia and their complications.
Owner:ZHUHAI HENGQIN NEW DISTRICT ZHONGZHU ZHENGTAI MEDICAL MANAGEMENT CO LTD

Method for synthetizing fenflumizole

The invention discloses a method for synthetizing fenflumizole and belongs to the technical field of organic chemical synthesis. The method comprises the following steps: under the action of a catalyst, reacting methyl 4-methoxybenzoate with 4-methoxyacetophenone to generate 1,3-bis(4-metoxybenzene)-1,3 diketone; reacting with tert-butyl nitrite to generate 1,2-bis(4-metoxybenzene)-1,2 diketone; and reacting with 2,4-difluorine benzaldehyde to generate 2-(2,4-difluorophenyl)-4,5-bis(methoxyphenyl)-1H-imidazole. By the adoption of the method, 1,2-diketone is prepared from 1,3-diketone, so that the use of KCN (potassium cyanide) can be avoided.
Owner:ZHEJIANG UNIV +1

Method for improving compounding stability of potassium 2-hydroxy-4-methoxybenzoate and tranexamic acid

The invention relates to the technical field of cosmetics, in particular to a method for improving compounding stability of potassium 2-hydroxy-4-methoxybenzoate and tranexamic acid. A light protecting agent is added to a potassium 2-hydroxy-4-methoxybenzoate and tranexamic acid compounding system, and the pH value of the system is controlled to 4.5-6.5. The light protecting agent is added, and the pH value of products is regulated, so that the problems that after being compounded, the potassium 2-hydroxy-4-methoxybenzoate and the tranexamic acid compound can generate the phenomenon of color changes after illumination is solved, the appearance and the color stability of products are effectively protected, and the usage amount of the potassium 2-hydroxy-4-methoxybenzoate and the usage amount of the tranexamic acid can achieve relative high dosage. The appearance and the color stability of prepared products are obviously improved. Within a long time, obvious color changes are not generated, test proves that the method is effective on delaying a photochemistry reaction due to interaction of the potassium 2-hydroxy-4-methoxybenzoate and the tranexamic acid, and the products can maintain durable stability, so that consumers can obtain good using experience.
Owner:上海珈凯生物股份有限公司

Preparation method of micamba methyl ester

The invention provides a preparation method of micamba methyl ester. The preparation method comprises the steps as follows: A) salicylic acid and bromine are subjected to a reaction in concentrated sulfuric acid, 5-bromosalicylic acid is obtained; B) 5-bromosalicylic acid and chlorine are subjected to a chlorination reaction, 5-bromo-3,6-dichlorosalycylic acid is obtained; C) 5-bromo-3,6-dichlorosalycylic acid is subjected to a debromination reaction under the alkaline condition and under the action of metal powder, and 3,6-dichlorosalycylate is obtained; D) 3,6-dichlorosalycylate and halomethane are subjected to a methylation reaction in methanol and a quaternary ammonium salt phase transfer catalyst, and 3,6-dichloro-2-methyl methoxybenzoate is obtained; E) methanol is removed by distillation; F) a system after distillation is left to stand for laying, an organic phase is distilled, and dicamba methyl ester is obtained. By means of the preparation method, the yield and purity are higher, the route is simple and the production cost is low.
Owner:SHANDONG RUNBO BIOTECH CO LTD

Out of tank type electrochemical synthesizing method of p-methoxy phenylacetone

The invention discloses a tank-exterior electrochemistry composite technique of methoxylbenzyl-ketone that relates to electrochemistry technique field. Adopt Pt filament as positive pole and stainless fin as negative pole in bi-room electrolysis tank, acetic acid-acetic acid anhydride as disslovant, kalium acetate as electrolysis support, at certain temperature, lead acetate as reactor, electrolysis with constant electricity density acquiring lead tertraacetate, add all the obtained lead tertraacetate into anethole after the electrolysing is stopped and acquiring organic product after the reaction stops, hydrolytic decomposing with sulfuric acid , extract with diethyl ether and finally obtain the product acetone p-methoxybenzoate. The left lead acetate can be recycled after processing. The productivity of above technique is 52 to 62 percent. The invention has got advantages such as simple and easy reaction material, environmental reaction process, safe operation, high productivity and low cost, is a technique of high added value.
Owner:EAST CHINA NORMAL UNIV

Method for synthesizing anisic aldehyde by selective hydrogenation of methyl methoxybenzoate

The present invention relates to selective hydrogenation process of methyl methoxybenzoate to synthesize anisic aldehyde, and belongs to the field of fine chemical catalysis technology. The present invention features the multiple phase selective hydrogenation process to synthesize anisic aldehyde with methyl methoxybenzoate. The catalyst consists of transition metal oxide loaded onto active carbon, alumina, silica, diatomite or molecular sieve. Methyl methoxybenzoate and hydrogen are led continuous into fixed bed reactor and reacted at 300-600 deg.c to obtain anisic aldehyde in rather high selectivity. The anisic aldehyde product has high purity and contains no any halogen atoms, so that it may be used safely in medicine, cosmetics and perfume. In addition, the present invention has short technological process and no environmental pollution.
Owner:DALIAN UNIV OF TECH

Preparation method of methoxybenzoic acid

The invention discloses a preparation method of alkali metal methoxybenzoate shown in a formula B. The preparation method comprises the following steps: 1, under the protection of inert gas, performing nucleophilic substitution reaction on a compound A and sodium methylate in methanol, wherein the reaction temperature is 80-150 DEG C and the reaction pressure is 0.18-1.4 MPa; 2, directly mixing a solution obtained in the step 1 with alkali metal hydroxide and water, removing methanol, and performing hydrolysis reaction to obtain a compound B, wherein the reaction temperature is 90-190 DEG C, and alkali metal hydroxide is sodium hydroxide and / or potassium hydroxide; performing acidification reaction on the prepared compound B and acid to prepare methoxybenzoic acid shown in a formula C. According to the method, the raw materials are easily available, a low-price safe reagent is used, and a one-pot process is adopted; the method is low in alkali consumption, little in environmental pollution, easy to perform, high in yield and suitable for industrialized production.
Owner:联化科技(上海)有限公司 +2

Preparation method of dicamba

InactiveCN109761781AStable and efficient separationHigh yieldPreparation from carboxylic acid esters/lactones2-methoxybenzoateHalomethane
The invention provides a preparation method of dicamba. The preparation method comprises the steps as follows: A) 3,6-dichlorosalicylic acid is salified under an alkaline condition; B) 3,6-dichlorosalicylate and halomethane are subjected to a methylation reaction under the action of a catalyst, and 3,6-dichloro-2-methyl methoxybenzoate is obtained, wherein the catalyst comprises tertiary amine andquaternary ammonium salt; C) methyl 3,6-dichloro-2-methoxybenzoate is subjected to acidification and drying, and dicamba is obtained. A compound phase transfer catalyst is adopted in the etherification process, so that salicylic acid is completely converted into dicamba methyl ester, separation of oil and water phases is realized, alkaline hydrolysis and acidification routes in the prior art arereplaced by distillation and acidification, the production process in the whole process is simple, the product quality is good and industrial production is facilitated.
Owner:SHANDONG RUNBO BIOTECH CO LTD

Method for synthesizing 1-(3-ethyoxyl-4-methoxy)phenyl-2-methyl-sulfonyl ethylamine

The invention discloses a method for synthesizing 1-(3-ethyoxyl-4-methoxy)phenyl-2-methyl-sulfonyl ethylamine and belongs to the technical field of organic synthesis processes. The method comprises the following steps: taking 3-hydroxy-4-methoxybenzoic acid as a raw material, carrying out an esterification reaction to obtain 3-hydroxy-4-methoxybenzoate, reacting with bromoethane to obtain 3-ethyoxyl-4-methoxybenzoate, then reacting with dimethyl sulfone to obtain 1-(3-ethyoxyl-4-methoxy)phenyl-2-methyl sulfonyl ethyl ketone, and finally carrying out a reductive amination reaction with ammoniumformate, thereby obtaining the 1-(3-ethyoxyl-4-methoxy)phenyl-2-methyl-sulfonyl ethylamine.
Owner:CHANGZHOU UNIV

Choleretic drug alibendol preparation method

The invention belongs to the field of drug synthesis, and provides an alibendol preparation method, which comprises: selecting 2-hydroxy-3-methoxybenzaldehyde as a raw material, selecting an efficientoxidative esterification catalyst, carrying out one-step oxidative esterification to obtain methyl 2-hydroxy-3-methoxybenzoate, carrying out a reaction on the methyl 2-hydroxy-3-methoxybenzoate and allyl bromide under the action of an alkali to generate methyl 2-allyloxy-3-methoxybenzoate, carrying out a para Claisen rearrangement reaction on the methyl 2-allyloxy-3-methoxybenzoate at a high temperature to obtain methyl 2-hydroxy-3-methoxy-5-allylbenzoate, and carrying out an aminolysis reaction in ethanolamine to generate alibendol. Compared with the traditional synthetic process, the new process of the present invention has characteristics of simple synthesis steps, convenient post-treatment and good product quality, and is suitable for industrial production.
Owner:辽宁博美医药科技有限公司

Sympathetic inhibitor, and cosmetic composition, food, and sundry article containing the same

Disclosed are a sympathetic inhibitor allowing more effective inhibition of activity of a sympathetic nerve, as well as a cosmetic composition, a food, and a sundry article containing the same. Ethyl 4-methoxybenzoate is efficacious for quieting down the activity of the sympathetic nerve. The sympathetic inhibitor, the cosmetic composition, the food and the sundry article containing the same enable more effective inhibition of the activity of the sympathetic nerve.
Owner:SHISEIDO CO LTD

Preparation method and application of tri(2-methyl-2-phenylpropyl)tin 3, 5-dimethoxybenzoate complex

The invention discloses a preparation method and an application of a tri(2-methyl-2-phenylpropyl)tin 3,5-dimethoxybenzoate complex. The tri(2-methyl-2-phenylpropyl)tin 3, 5-dimethoxybenzoate complex is a complex represented by structural formula (I) shown in the description. The invention further discloses the preparation method of the tri(2-methyl-2-phenylpropyl)tin 3,5-dimethoxybenzoate complexand the application of the tri(2-methyl-2-phenylpropyl)tin 3, 5-dimethoxybenzoate complex in the preparation of antitumor drugs.
Owner:HENGYANG NORMAL UNIV

Process for preparing benzoic acid esters

There is provided a more industrially advantageous process for preparing novel pyridine derivatives expected to be used as medicines. A process for preparing 3-[(6-hydroxy-1-methyl-1H-benzimidazol-2-yl)methoxy]benzoic acid esters as intermediates with high quality, in short steps and in a high yield, as well as novel benzoic acid esters as their precursors and a process for preparing the same.
Owner:DAIICHI SANKYO CO LTD

Preparation method of multifunctional light scattering film

The invention belongs to the technical field of films, and particularly relates to a preparation method of a multifunctional light scattering film. The method comprises the steps of sequentially carrying out vacuum evaporation of 2, 7-dimethyl-3- (2, 4-dichlorophenyl) -paryzolo [1, 5-a] pyrimidine-6-formic acid, 6-chorine-2-methyl-3- (5-methoxy-2-hydroxylphenimethylamine) -4 (3H) -quinazolinone, 2-chlorine-5- (5-mercapto-4-isopropyl-4H-1, 2, 4-triazole-3-base) benzenesulfonamide, 4- acetoxy-3- Berberine methoxybenzoate on a glass plate, and preparing the multifunctional light scattering film,wherein the light transmittance of the film is 86%-91%, and the haze is 89%-93%; and the color of the multifunctional light scattering film is orange, yellow and green after irradiating white light, ultraviolet light with the wavelength of 365nm and ultraviolet light with the wavelength of 254nm for 60 seconds.
Owner:TAICANG BIQI NEW MATERIAL RES & DEV

Tin-oxygen-heterocycle-structured dibutyltin 2,4,5-trifluoro-3-methoxy-benzoate complex as well as preparation method and application thereof

The invention discloses tin-oxygen-heterocycle-structured dibutyltin 2,4,5-trifluoro-3-methoxy-benzoate, which is a complex having the structural formula (I) (shown in the description), wherein R represents n-butyl. The invention further discloses a preparation method of the complex and application of the complex in the preparation of antitumor drugs.
Owner:HENGYANG NORMAL UNIV

Special self-cleaning badminton sock composite yarn and preparation method thereof

InactiveCN110306269AGood tensile and wear resistanceSoft and comfortableCarbon fibresYarnYarnPolyester
The invention relates to the field of textiles, in particular to a special self-cleaning badminton sock composite yarn and a preparation method thereof. The composite yarn comprises, by weight, 40-60parts of bamboo fibers, 10-20 parts of polyester fibers, 5-10 parts of bamboo carbon fibers, 2-6 parts of ramie fibers, 20-30 parts of nano-titanium dioxide photocatalyst micro-emulsion, 10-20 parts of methyl 3-methoxybenzoate, 200-300 parts of deionized water, 15-25 parts of tween 80, 3-9 parts of cinnamyl aldehyde and 2-8 parts of glycerin monostearate. The prepared yarn is good in tensile and abrasion resistance and soft and comfortable in hand feeling. A badminton sock prepared from the yarn can meet moisture absorption and sweat releasing requirements of athletes, the nano-titanium dioxide photocatalyst micro-emulsion is sprayed, a photocatalyst layer can be formed on the surface of the yarn, harmful organic matters adhered on the yarn can be decomposed into carbon dioxide and water under sunshine, light cleaning effect is achieved, and the yarn is easily cleaned.
Owner:湖南莎丽袜业股份有限公司

A kind of preparation method of methyl 3-bromo-4-difluoromethoxybenzoate

The present invention discloses a preparation method for 3-bromo-4-difluoromethoxy methyl benzoate represented by a formula 3. The method comprises: mixing a compound 2, sodium chlorodifluoroacetate, an inorganic weak base and an organic solvent, and carrying out a reaction at a temperature of 85-110 DEG C to obtain the finished product, wherein a molar ratio of the compound 2 to the sodium chlorodifluoroacetate to the inorganic weak base to the organic solvent is 1.0:(1.5-2.5):(1.0-2.0):(15-25), a reaction temperature is 85-110 DEG C, the organic solvent is one or a plurality of materials selected from DMF, isopropanol and 1,4-dioxane, and the inorganic weak base is one or a plurality of materials selected from potassium carbonate, cesium carbonate and sodium carbonate. The preparation method has characteristics of high conversion rate, simple post-treatment, high product yield and high product purity, and is suitable for industrial production.
Owner:SHANGHAI INST OF PHARMA IND +1
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products