46 results about "Hydronaphthalene" patented technology

The invention discloses a method for preparing a tetrahydro-1,5-naphthyridine compound. The method comprises the following steps: carrying out an addition reaction between a compound with the structure shown as a formula (1) and hydrogen in the presence of a chiral catalyst, wherein the chiral catalyst is a coordination complex with a structure shown as a formula (2). The invention also provides a chiral product of the tetrahydro-1,5-naphthyridine compound prepared by the method. The proper compound with the structure shown as the formula (1) is selected as a substrate, the proper coordination complex with the structure shown as the formula (2) is selected as the chiral catalyst, and selective hydrogenation reduction of the 1,5-naphthyridine compound with the structure shown as the formula (1) is realized by adopting hydrogen, so that the chiral product of the tetrahydro-1,5-naphthyridine compound is prepared at low cost. The chiral product of the tetrahydro-1,5-naphthyridine compound prepared by the invention can serve as a structure block of bioactive compounds and chiral drugs.

The invention discloses a preparation method of a tetrahydro 1, 8-naphthyridine compound. The preparation method comprises the following steps: under the existence of a chiral catalyst, enabling a compound with the structure shown in the formula (1) (in the description) and hydrogen to be subjected to addition reaction, wherein the chiral catalyst is a coordination compound with the structure shown in the formula (2) (in the description). The invention further provides a chiral product of the tetrahydro 1, 8-naphthyridine compound, prepared through the preparation method. According to the invention, the proper compound with the structure shown in the formula (1) (in the description) is used as a substrate, and the proper coordination compound with the structure shown in the formula (2) (in the description) is used as the chiral catalyst to perform selective hydrogenation reduction on 1, 8-naphthyridine compound with the structure shown in the formula (1) by adopting hydrogen, so that the chiral product of the tetrahydro 1, 8-naphthyridine compound is prepared with low cost. The chiral product of the tetrahydro 1, 8-naphthyridine compound can be used as a biologically active compound and a structural building block of a chiral drug.

An application of the oxalate in preparing norambrether or releasing the norambrether to the smoke of cigaretter is disclosed. Said oxalate may be decahydro-2-hydroxy-2,5,5,8a-tetramethyl-naphthal eneethanol or 2-hydroxy-2,5,5,9-tetramethyl decalyl ethanol. It can be proportionally added to cigarette, or can be decomposed to obtain norambrether.

The present invention belongs to the field of organic chemistry and relates to a multi-substituted hydrogenated naphthalene compound, the preparation methods and uses. Specifically, the present invention relates to a chiral multi-substituted ten-hydrogen and / or eight-hydrogen naphthalene compound, the synthetic method and uses. The present invention aims to provide a chiral multi-substituted ten-hydrogen and / or eight-hydrogen naphthalene compound; the oleanane-type or usu-type five-ring triterpenoid compound is used as a raw material for preparing the compound. The multi-substituted ten-hydrogen and / or eight-hydrogen naphthalene compound of the present invention can be used for synthesis of drugs or spices containing multi-hydrogen naphthalene fragments and the analogues. The method of the present invention is simple and easy, low in cost, high in production rate, and can realize industrialization.

The invention relates to a preparation method of industrial musk tonalide, which comprises the following steps: carrying out Friedel-Crafts alkylation by using p-isopropyl toluene and 2,3-dimethyl-1-butene as raw materials and using tertiary butyl chloride as a hydrogen absorption agent to synthesize an intermediate 1,1,3,4,4,6-hexamethyl tetrahydronaphthalene; and in a dichloromethane solvent, carrying out Friedel-Crafts alkylation on the intermediate used as the raw material and acetyl chloride, thereby obtaining the product musk tonalide (7-acetyl-1,1,3,4,4,6-hexamethyl tetrahydronaphthalene, AHMT). Compared with the existing method and technology, the method provided by the invention is simple to operate, has the characteristics of high reaction speed, high yield and the like, and realizes industrial production; and the product can be simply purified by thermally dissolving out pigments by using anhydrous alcohol without distillation or rectification.

The invention belongs to the technical field of medicine and discloses bexarotene hydroximic acid as well as a preparation method and application thereof. The formation of the compound is as shown in the picture and the objective compound is prepared mainly by taking 1,1,4,4,6- pentamethyl-1,2,3,4-tetrahydronaphthalene as the initial material through the steps of Friedel-Crafts acylation, Wittig reaction and condensation reaction. The method is simple in operation, convenient in post-processing and high in yield. The objective compound has good inhibitory action on various cancer cells by the multiple action mechanisms of bonding the retinoic acid X receptors and restraining the histone deacetyltransferases, and the anti-cancer activity of the bexarotene hydroximic acid is obviously better than that of bexarotene. Therefore, the bexarotene hydroximic acid can be applied to treatment of cancers.

The invention discloses a separating and purifying device and process for heavy component residual liquid of a hydrogenation process of coking crude benzene, belonging to the technical field of fractioning separation. The separating and purifying device of the invention comprises a tower kettle, a batch fractioning tower, a tower top fraction storage tank and a vacuum pump, wherein the batch fractioning tower is connected with the tower kettle; a condenser is arranged at the tower top of the batch fractionating tower; and the vacuum pump is respectively connected with the condenser and the tower top fraction storage tank through a buffer tank. The process comprises the following steps: when the tower top pressure is 10.0-15.0kPa, and the tower top temperature is 115.0-120.0 DEG C, collecting indan from the tower top by a reflux ratio of 4-5; after the indan is collected, when the tower top pressure is 10.0-15.0kPa, and the tower top temperature is 125.0-130.0 DEG C, collecting tetraline from the tower top by the reflux ratio of 8-10; and finally when the tower top pressure is 10.0-15.0kPa, and the tower top temperature is 155.0-160.0 DEG C, collecting naphthalene from the tower top by a reflux ratio of 4-5. The purity of the indan is 99.0wt%, the purity of the tetraline is 99.5wt%, and the purity of the naphthalene is 98.0wt%.

A method of preparing (S)-2-amino-5-methoxytetralin hydrochloride[(S)-2-amino-5-methoxyl-1,2,3,4-tetrahydronaphthalene hydrochloride], comprising the steps of: (1) producing a compound (I) by addition-elimination reaction of 5-methoxy-2-tetralone and R-(+)-a-phenylethylamine; (2) producing a compound (II) by reduction reaction of the compound (I) with a reducing agent; and (3) producing a compound (II) hydrochloride by reacting the compound (II) with a salt-forming agent, then carrying out reduction reaction with a palladium-carbon catalyst to produce (S)-2-amino-5-methoxytetralin hydrochloride. The method can significantly increase the yield of (S)-2-amino-5-methoxytetralin hydrochloride with short synthetic path, low preparation cost and less pollution, which is environmentally friendly and is suitable for medical industrialized production. The structural formulae of the compound (I) and the compound (II) are:resepectively.

A process for preparing indanylamine and aminotetralin derivatives from indanone or tetralone oximes by acylating the oximes with an organic anhydride, followed by catalytic hydrogenation in the presence of an organic anhydride with subsequent hydrolysis is described. The process is commercially feasible providing indanylamine and aminotetralin derivatives in high yield that are useful as intermediates in the production of therapeutically active compounds. Also described are novel intermediates, 1-indanone O-acetyl oximes and 1-tetralone O-acetyl oximes.

The invention discloses a synthesis strategy for constructing a 2-cyanoalkyl sulfonyl substituted 3,4-dihydronaphthalene compound by taking MCPs, a cyclobutanone oxime ester compound and K2S2O5 as rawmaterials through visible light catalysis, wherein two carbon-carbon sigma bonds are broken in a one-pot reaction to form a carbon-carbon bond and two carbon-sulfur bonds. According to the invention,cyanoalkyl free radicals are formed to capture SO2, and subsequently sulfonyl free radicals are formed to carry out ring-opening and cyclizing on MCPs; and the synthesis method disclosed by the invention has the advantages of mild reaction conditions, simplicity, high efficiency, easily available raw material sources, wide substrate application range and high target product yield.

The invention relates to a synthetic method of 1, 1, 3, 5-tetramethyl-3-isopropyl hydrindene. The synthetic method specifically comprises the following steps: S1, uniformly mixing p-cymene, chlorotert-butane and 2, 3-dimethyl-1-butene, dropwise adding an obtained mixed solution into a reaction kettle filled with cyclohexane and aluminum trichloride, stirring for reaction, washing with water and alkali for elution, and rectifying to remove p-cymene, so as to obtain a 1, 1, 3, 4, 4, 6-hexamethyltetrahydronaphthalene crude product; S2, transferring the 1, 1, 3, 4, 4, 6-hexamethyl tetrahydronaphthalene crude product obtained in the step S1 into an isomerization kettle, then adding dichloroethane and aluminum trichloride, and carrying out stirring, heating and reflux reaction; S3, washing a product obtained after the isomerization reaction with water and alkali until the product is neutral, desolventizing to remove dichloroethane, transferring an obtained desolventized 1, 1, 3, 5-tetramethyl-3-isopropyl hydrindene crude product into a crystallization kettle, adding a crystallization solvent, and recrystallizing for multiple times to obtain the 1, 1, 3, 5-tetramethyl-3-isopropyl hydrindene. According to the synthetic method of the 1, 1, 3, 5-tetramethyl-3-isopropyl hydrindene, provided by the invention, the yield of a target product is improved, and the purification difficulty is reduced.

The invention relates to a hydrofining method of crude 2, 6-naphthalic acid, and mainly solves the problem that in the prior art, during hydrofining of crude 2, 6-naphthalic acid, a large amount of impurity 2, 6-dicarboxyl-1, 2, 3, 4-tetrahydronaphthalene is generated. The crude 2, 6-naphthalic acid hydrofining method comprises the following steps: in the presence of a hydrofining catalyst, water is taken as a solvent, crude 2, 6-naphthalic acid reacts with hydrogen to obtain refined 2, 6-naphthalic acid, the catalyst comprises a carrier and a noble metal loaded on the carrier, the noble metal comprises palladium, and the noble metal comprises palladium. The average grain size of palladium is 2-5nm through X-ray diffraction analysis, so that the problem is well solved, and the method can be used for producing refined 2, 6-naphthalic acid.

A process for synthesizing naphthalene alkylmethyltetrahydride from alkylbenzene and isopentandiene includes alkylation reaction between C1-C5 alkylbenzene and isopentandiene under the existance of Lewis acid or Y-type molecular sieve to obtain pentenylalkyl benzene, and cyclizing reaction under existance of Y-type molecular sieve. Its advantages are simple process and low cost.

The present invention is a method for removing sulfur from liquid hydrocarbon feedstocks and for performing hydrogenation reactions in sulfur-contaminated feedstocks, including the hydrogenation of naphthalene in the presence of sulfur compounds, using catalysts or adsorbents comprising metal oxide nanowires decorated with reduced catalytically-active metal particles. In a preferred embodiment, the adsorbent comprises zinc oxide nanowires decorated with catalytically-active metals selected from nickel, cobalt, molybdenum, platinum, palladium, copper, oxides thereof, alloys thereof, and combinations thereof. In some embodiments, the sulfur is removed through a desulfurization process without an external hydrogen supply. The process is effective for the removal of sulfur from diesel fuels and liquid fuel streams, and for deep desulfurization of natural gas streams. The process is also effective for the selective hydrogenation of naphthalene to tetralin in the presence of sulfur compounds.

The invention discloses a preparation method of a tetrahydronaphthalene benzamide key intermediate. The preparation method comprises the following steps: adding a compound a into a reaction container, adding a reaction solvent for dissolving, and adding 3-iodine-4-methylaniline while controlling the temperature at 5-45 DEG C; vacuumizing the obtained reaction system, introducing nitrogen for protection, controlling the temperature at 15-25 DEG C, slowly dropwise adding a catalyst, heating the reaction system to 80-110 DEG C after dropwise adding, and reacting for 3-4 hours to obtain a reaction mixture; and adding an extraction system into the obtained reaction mixture for extraction, separating and taking an organic phase, washing, drying and evaporating or concentrating and crystallizing to obtain the tetrahydronaphthalene benzamide key intermediate. According to the method disclosed by the invention, the reaction time is greatly shortened, the yield is improved, the use of a catalyst is reduced, byproducts in the reaction are reduced, and the cost is greatly saved.

The invention relates to a carbon monoxide feed gas dehydrogenation separation purification process which comprises the following two steps: hydrogen absorption: under the action of a hydrogen absorption catalyst, absorbing hydrogen from carbon monoxide raw material gas by adopting organic liquid to obtain hydrogen absorption liquid and carbon monoxide treatment gas, wherein the organic liquid isselected from at least one of cyclohexane, tetrahydronaphthalene, carbazole and ethyl carbazole, and dehydrogenation: dehydrogenating the hydrogen absorption liquid under the action of a dehydrogenation catalyst to obtain a dehydrogenation liquid and purified hydrogen. According to the technology, organic matter is used for hydrogen absorption and hydrogen desorption, the hydrogen content in the carbon monoxide treatment gas is low and is smaller than or equal to 85 ppm, the purity of purified hydrogen is larger than or equal to 98%, and the purified hydrogen can be recycled. The method is insensitive to the concentration of hydrogen in the feed gas and can be used for treating carbon monoxide feed gas with the hydrogen volume ratio not larger than 20%, and organic liquid is recycled.

The invention discloses a method for efficiently synthesizing a (1R,2S)-1,2-dialin derivative. The method is characterized by carrying out asymmetric cis-form ring opening on nitrogen / oxygen benzene and norbornene by taking an oximes compound as a nucleophilic reagent in an organic solvent system and under an inertial atmosphere, thus obtaining a target object-the (1R,2S)-1,2-dialin derivative, wherein a reaction formula of the (1R,2S)-1,2-dialin derivative is as shown in the description. According to the method disclosed by the invention, efficient synthesis of the (1R,2S)-1,2-dialin-1,2-diamine derivative through one-step simple reaction by taking the simple oximes compound, the nitrogen / oxygen benzene and norbornene compounds as raw materials is realized for the first time, wherein a hydroxyl group (-OH) or amino group (-NH2) is used as a substituent group.

The invention relates to a method for one-pot synthesis of high-density alkyl decahydronaphthalene aviation kerosene from biomass conjugated diene and p-benzoquinone. The process is completed in one pot through two steps, in the first step, conjugated diene and p-benzoquinone are subjected to a Diels-Alder reaction under the thermal action to generate a ring adduct, and in the second step, alkyl decahydronaphthalene is synthesized through hydrodeoxygenation under the action of a bifunctional catalyst. According to the method, the separation and purification steps of an intermediate product are omitted in a one-pot manner, so that the purposes of reducing product loss, energy cost and waste output are achieved, and direct conversion from a lignocellulose platform compound to a high-density aviation kerosene alkyl decalin alkane compound is realized.