121 results about "2-Pentanone" patented technology

A process for producing high yields of gamma -hexalactone and 2-pentanone from the corresponding hexanoic acid starting material is carried out with high amounts of oxygen and sugar in the presence of a mold microorganism. Fragrance compositions and foodstuff compositions are augmented and enhanced by the presence of the product compounds.

A photoimagable composition suitable for use as a negative photoresist comprising: (A) at least one epoxidized polyfunctional bisphenol A formaldehyde novolak resin; (B) at least one polycaprolactone polyol reactive diluent, wherein the amount of component (A) is from about 95% to about 75% by weight of the sum of (A) and (B) and the amount of component (B) is from about 5% to about 25% by weight of the sum of (A) and (B); (C) at least one photoacid generator in an amount from about 2.5 to about 12.5 parts per hundred parts of resin and reactive diluent, which initiates polymerization upon exposure to actinic radiation; and (D) a sufficient amount of solvent to dissolve (A), (B) and (C); wherein the solvent comprises 2-pentanone, 3-pentanone, and 1,3-dioxolane and mixtures thereof.

The invention discloses mixed stewed pork essence which consists of furanone, ethyl maltol, 2-acetylpyrazine, methyl cyclopentenolone, difurfuryl sulfide, 3-sulfydryl-2-butanol, 2-methyl-3-furan mercaptan, di(2-methyl-3-furan mercaptan)-disulfide, methyl(2-methyl-3-furan mercaptan)-disulfide, acetic acid, 3-sulfydryl-2-butanone, 3-propionaldehyde, thiophane-3-acetone, 2,3,5-trimethyl pyrazine, counter,counter-2,4-decadiene aldehyde, furfuryl disulfide, furfurylmercaptan, anise camphor, anisic aldehyde, pepper essential oil, 2-acetyl thiazole, delta-dodecalactone, 4-methyl-5(beta)-hydroxyethyl thiazole acetate, onion oil alcohol, 4-methyl-4-bran sulfenyl-2-pentanone and glycerol triacetate. The mixed stewed pork essence is high in biofidelity and mellow and fine in fragrance, has a good application effect and is economical and practical.

The invention relates to a chicken flavor, including the following ingredients according to weight percentage: 0.5-1.0 part of ethyl maltol, 0.05-0.1 part of 2-acetylpyrazine, 0.1-0.2 part of clove oil, 0.05-0.1 part of cassia oil, 0.3-0.4 part of ginger essential oil, 0.2-0.3 part of star anise oil, 0.05-0.2 part of 3-methylthio-propanal, 0.01-0.1 part of (E,E)-2,4-decadienal, 0.2-0.4 part of 4-methyl-4-furfurylthio-2-pentanone, 0.05-0.2 part of tetrahydrothiophen-3-one, 0.01-0.1 part of 2,5-dimethyl-2,5-dihydroxy-1,4-disulfocyclohexane, 0.1-0.3 part of bis(2-methyl-3-furyl)disulfide, 0.01-0.1 part of 2-furfuryl monosulfide, 0.01-0.05 part of 2-Methyl-3-tetrahydrofuranthiol solution and 96.45-98.36 parts of soy salad oil. The chicken flavor has nature stewing chicken fragrance and taste as well as good temperature tolerance.

The present invention provides a 5-chloro-2-pentanone preparation method, which comprises that: 2-methyl furan is subjected to a hydrogenation reaction in the presence of a hydrogenation catalyst and hydrogen gas to prepare 2-methyl-4,5-dihydrofuran, and the 2-methyl-4,5-dihydrofuran and hydrochloric acid are subjected to a ring opening chlorination reaction to obtain the 5-chloro-2-pentanone. According to the present invention, 2-methyl furan is adopted as the raw material, the reaction steps are simple and easy to operate, no wastewater is generated during the production process, and environmental protection requirements are met; the hydrogenation catalyst, the distillate and the hydrochloric acid can be recycled so as to substantially reduce the production cost, and the prepared product has characteristics of high yield and high purity; and compared with the conventional process, the preparation method of the present invention has characteristics of complete elimination of influence of hydrochloric acid on the catalyst, improvement of the catalyst utilization rate, and substantial reduction of the 5-chloro-2-pentanone production cost.

It is an object of the present invention to provide an inexpensive and efficient industrial method for obtaining (S)-2-pentanol, (S)-2-hexanol, 1-methylalkyl malonic acid and 3-methyl carboxylic acid at a high optical purity. The present invention provides a method of producing (S)-2-pentanol or (S)-2-hexanol which comprises allowing certain types of microorganisms or transformed cells, a product obtained by treating said microorganisms or cells, a culture solution of said microorganisms or cells, and/or a crude purified product or purified product of a carbonyl reductase fraction obtained from said microorganisms or cells, to act on 2-pentanone or 2-hexanone.

A catalyst used for synthesizing 2-pentone from ethanol is prepared from zirconium oxide, manganese oxide, zinc oxide, less noble metal (Pt, Pd, Rh, etc) and less assistant (Li, Na, K, Mg, etc) through mixing three oxides, dipping assistant, calcining, dipping noble metal, and calcining. It has high activity, selectivity and stability.

The invention relates to high-energy welding-cutting gas, which relates to welding-cutting gas, and aims to solve the problems of environment pollution, high energy consumption and high cost existing when acetylene gas is used as welding-cutting gas. The high-energy welding-cutting gas is formed by mixing nano flame accelerator with natural gas, wherein the nano flame accelerator is formed by mixing jet fuel, ethanol, n-butyl alcohol, ethyl acetate, ethylene glycol monobutyl ether, tert-butyl hydroperoxide, 2-pentanone, nanometer aluminium oxide, nanocrystalline iron oxide and borane-pyridinecomplex. The high-energy welding-cutting gas has the advantages that: the nano flame accelerator is adopted, so that the flame of the natural gas is concentrated, the flame temperature rises, the useefficacy of acetylene gas is achieved, the cutting quality of workpieces is improved, safety is realized without tempering, the gas consumption and the oxygen consumption are greatly reduced, a bottle of high-energy welding-cutting gas with the volume being 3 cubic meters can replace a bottle of acetylene gas with the weight being 3 kg for use, the cost of the welding-cutting gas is one fifth of the cost of the acetylene gas, and the main component of the high-energy welding-cutting gas is the natural gas, so that the environment pollution is reduced compared with the acetylene gas. The invention is mainly used for preparing the welding-cutting gas.

The invention relates to a catalyst for synthesizing 3-pentanone, and belongs to the technical field of preparation of catalysts for fine chemical products. The catalyst consists of an active composition, an auxiliary agent and a carrier, wherein the active composition is one or more of lanthanum rare earth oxide and actinium rare earth oxide; the carrier is one or more of zirconia, alumina, titania and silicon dioxide; the weight ratio of the active composition to the carrier is 5-80:95-20; and the auxiliary agent is one or more alkali metals or alkaline earth oxides and is 0.1 to 5 weight percent of the total weight of the active composition and the carrier. The catalyst not only maintains the activity of the prior catalyst, but also overcomes the defects of the prior rare earth catalyst, achieves the aims of inhibiting the isomerization reaction and reducing the content of 2-pentanone and methyl isopropyl ketone in the reaction products, and greatly reduces the separation difficulty of the 3-pentanone.

The invention discloses a synthesis method of a 3'-acyl-2,4'-dihydroxyl diphenyl ketone compound, and belongs to the technical field of organic synthesis. The key point of the technical scheme of the invention is as follows: the synthesis method of the 3'-acyl-2,4'-dihydroxyl diphenyl ketone compound particularly comprises the following processes: disoolving a 3,4-diene-2-pentanone compound and a 3-formyl chromone compound into a first solvent, performing stirring reaction at a temperature of 50 to 80 DEG C under the acidic condition, adding a second solvent and alkali, and performing stirring reaction at 60 to 100 DEG C to prepare the 3'-acyl-2,4'-dihydroxyl diphenyl ketone compound. The 3'-acyl-2,4'-dihydroxyl diphenyl ketone compound is synthesized through one-pot multi-step cascade reaction of the 3,4-diene-2-pentanone compound and the 3-formyl chromone compound; the synthesis method of the 3'-acyl-2,4'-dihydroxyl diphenyl ketone compound has the advantates of simplicity and convenience in operation, mild condition, wide application range of substrates and the like, and is suitable for industrialized production.

A process for synthesizing pentone from ethanol features the reaction between ethanol and catalyst K-Pd/ZrO2/MnO/ZnO in initial gas. Its advantages are high conversion rate (100%) and selectivity. Its separation method is distilling.

The invention provides a visual array chip for gas analysis and application thereof. According to the visual array chip, functional modules from No.1 to No.36 are arranged on a substrate according to an array distribution mode, and the functional modules are prepared by coating the substrate with porphyrin and dye modified by gold nano-particles, porous organic silicate, plasticizer and materials having specific response to aldehyde volatile organic compounds. The visual array chip can be used for detecting and analyzing at least one volatile gas in benzene, methylbenzene, p-xylene, trimethylbenzene, trichlorofluoromethane, propyl aldehyde, hexanal, acetaldehyde, heptanal, acetone, 2-pentanone, tetrahydrofuran, heptane, decane, undecane, 1-hexene, isoprene, styrene, acetic acid, propionic acid, ethylenediamine, tetramethylethylenediamine, acetonitrile, propyl alcohol, thiol and butyl acetate compounds. The chip can be used for detecting multiple gas ingredients, has high sensitivity for detected objects with low detection limit, and can reach the ppbv detection level.

The present invention relates to a process for producing an optically active 1,4-pentanediol by asymmetrically reducing 5-hydroxy-2-pentanone, which is easily available at low cost. The present invention also relates to a process for producing an optically active 1-substituted 2-methylpyrrolidine including sulfonylating the optically active 1,4-pentanediol to convert it to an optically active sulfonate compound, and reacting the compound with an amine. According to the processes of the present invention, an optically active 1,4-pentanediol and an optically active 1-substituted 2-methylpyrrolidine, which are useful as an intermediate for medicines and an intermediate for agricultural chemicals, can be simply produced from an inexpensive starting material.

The invention discloses a synthetic method of 5-(N-ethyl-N-2-ethylol amine)-2-amylamine. The method comprises the following steps: (1) the preparation of a catalyst, to be specific, dispersing and dissolving nitrate into an organic solvent, adding oxide or nanopowder of carbonate into the organic solvent, after ultrasonic stirring, evaporating the organic solvent to dryness, carrying out vacuum drying and grinding the dried solvent into fine powder to obtain the catalyst; (2) adding xylene, 5-chlorine-2-pentanone and N-ethylethanolamine in a reaction flask in sequence, stirring the materials, adding the prepared catalyst, heating the flask to increase the temperature till reflux occurs, cooling the heated materials to room temperature, filtering the materials to obtain a filtrate, fractionating the filtrate to obtain 5-(N-ethyl-N-2-ethylol amine)-2-pentanone; (3) putting 5-(N-ethyl-N-2-ethylol amine)-2-pentanone in a hydrogenation flask, adding aminomethanol and raney nickel to perform reaction under hydrogen pressure; after the reaction, displacing the hydrogen and ammonia in the system with nitrogen, filtering the reaction liquid to obtain a filtrate, fractionating the filtrate to obtain 5-(N-ethyl-N-2-ethylol amine)-2-amylamine. The method is high in conversion rate, simple and convenient to operate, high in yield, low in cost, easy for industrial production, safe and environment-friendly.

The invention discloses synthesis of a novel catalyst and an application method thereof in catalyzing condensation of acetone and hydroxyaldehyde. The method comprises the following steps: adding acetone into a distillation kettle connected with a reactor and an apparatus for refluxing to remove water; then adding little catalyst into the reactor, carrying out reflux reaction for a certain time ata certain temperature when mixing, sampling to analyze; when the reaction is balanced, ending the reaction to obtain the product in the reaction kettle. The substance in the reactor is material acetone that is not adequately reacted and can be used as the reactant of next batch of reaction.

The invention relates to the technical field of chemical synthesis, and particularly discloses a preparation method of 2-chloro-1-(1-chlorocyclopropyl) acetone. The preparation method comprises the following steps: enabling alpha-acetyl-gamma butyrolactone and hydrochloric acid to have an open-loop decarboxylic reaction to obtain 5-chloro-2-pentanone; adding the 5-chloro-2-pentanone and a catalystinto an alkaline solution, implementing a cyclization reaction, obtaining cyclopropyl methyl ketone; implementing a chlorination reaction with a chloride agent to obtain the 2-chloro-1-(1-chlorocyclopropyl) acetone. The reaction steps of the provided method are less, the reaction period is short, the yield is more than 70%, and the content of the 2-chloro-1-(1-chlorocyclopropyl) acetone in a product is more than 95%.

The invention relates to a method of preparing 2-pentanone from ethanol. According to the method, CeO2 is taken as the catalyst, in a fixed bed reactor, in an inert gas atmosphere, ethanol is taken as the raw material, reactions are carried out at a temperature of 200 to 600 DEG C under a normal pressure; the liquid hourly space velocity (LHSV) of the reactions is 0.1-6.0 g<cat><-1>h<-1>, and the gas space velocity of the reactions is 2000 to 8000 mL.g<cat><-1>h<-1>. The method can efficiently convert cheap ethanol into 2-pentanone in one step. The ethanol conversion rate can reach 92.8%. The selectivity of 2-pentanone is 36.8%. Moreover, the used catalyst raw materials are cheap and easily-available, the preparation method is simple, a normal pressure reaction technology is adopted, the operation is easy, and the method can be applied to the industrial application.

The invention relates to a preparation method of a cyclopropyl acetylene important intermediate cyclopropylmethyl ketone. The invention adopts a technical scheme that: 5-chloro-2-pentanone is adopted as an initial raw material; under an alkaline condition and in a multistage reactor, a reaction is carried out with a reactive distillation technology, wherein a reaction temperature is controlled at 90-150 DEG C; and cyclopropylmethyl ketone is obtained in the multistage reactor. According to the invention, the reaction is carried out with the reactive distillation technology. Reaction and distillation are carried out simultaneously, such that the reaction process is simplified. Therefore, the operation is simple, and reaction can be continuously carried out. A cyclization reaction is carried out in the multistage reactor, such that space-time yield and selectivity of the reaction are improved. The reaction is carried out with the reactive distillation technology, such that reaction product is continuously removed, and reaction conversion rate is greatly improved. Because reaction selectivity and conversion rate are improved, three-waste production is greatly reduced, original steps of stratification and extraction are eliminated, and cost is reduced. The method is a green synthesizing process.