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31 results about "Amberlyst-15" patented technology

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High-yield levulinic acid ester preparation method under catalysis of solid acid

The invention discloses a high-yield levulinic acid ester preparation method under catalysis of solid acid and belongs to the field of organic synthesize. The method comprises the following steps: uniformly mixing 1 part of sugar, 10-100 parts of alcohol, 0.01-0.2 part of acid B and 0.1-1 part of acid L, and performing reaction under the temperature of 130-190 DEG C for 1-20 h to obtain a levulinic acid methyl ester solution, wherein the acid L is stanniferous molecular sieve, and the acid B is SBA-15-SO3H, Carbon-SO3H or Amberlyst-15. According to the method, the carbohydrate is low in cost and easy to obtain; with the acid B and acid L which can be used repeatedly, the catalysis effect basically remains the same; the levulinic acid ester compound prepared in one step can be widely applied to industries of food additives, essence spices, chemical reaction intermediates, gasoline, diesel-dopes and the like.
Owner:GUANGZHOU CHEM CO LTD CHINESE ACADEMY OF SCI

Preparation of quinoxaline derivatives

The invention discloses a preparation method of a quinoxaline derivative. The method is characterized by condensing an o-diamino compound with an o-dicarbonyl compound in a polar solvent in the presence of catalyst Amberlyst-15 or NKC-9 dry hydrogen catalyzed resin Styrene-DVB to prepare the quinoxaline derivative. The preparation method takes ordinary tap water instead of a toxic organic solvent as the solvent for a condensation reaction to obtain the quinoxaline derivative with high yield and high content. The catalyst can be recovered and can be reused for at least three times in a condition of no loss of the catalytic activity, thus effectively reducing the production cost. The preparation method of the quinoxaline derivative has the advantages of simple process operation, no environment pollution, and is fit for large-scale industrialized production.
Owner:TIANJIN NORMAL UNIVERSITY

Method used for catalyzed synthesis of tert-butyl acrylate

The invention relates to a method used for catalyzed synthesis of tert-butyl acrylate. The method comprises following steps successively:1) acrylic acid, a catalyst combination, a polymerization inhibitor A, and a polymerization inhibitor B are delivered into a sealed reaction kettle, and liquefied isobutylene is added dropwise for esterification, wherein the catalyst combination is composed of nanosolid superacid SO<4><2-> / SnO<2>, Amberlyst-15, D001 resin, and NKC-9 resin; 2) after adding, heat preservation is carried out; 3) after heat preservation, the sealed reaction kettle is subjected to pressure relief, an obtained mixture is subjected to filtration, and an obtain liquid ingredient is pumped into a rectifying tower; and 4) by-products tert-butyl alcohol, diisobutylene, and the target product tert-butyl acrylate are obtained via separation successively. Yield of tert-butyl acrylate is higher than 98%; reuse ratio of the catalyst is high; the method is simple; and no pollution is caused.
Owner:徐德良 +1

Method for preparing 5-ethoxymethylfurfural by glucose

The invention discloses a method for preparing 5-ethoxymethylfurfural by glucose. The method comprises the following steps of using the glucose as a reaction primer, using an anhydrous ethyl alcohol-dimethyl sulfoxide cosolvent system as a reaction medium, and using combination of aluminum trifluoromethanesulfonate and ion exchange resin Amberlyst 15 as a synergistic catalyst, so as to form a conversion reaction system; reacting at the temperature of 140 to 160 DEG C, so as to obtain the 5-ethoxymethylfurfural. The dimethyl sulfoxide is used as a cosolvent, so as to effectively inhibit the generation of side reaction; the glucose is converted into the target product at high selectivity, namely the 5-ethoxymethylfurfural; the maximum yield rate reaches 48.8%. The preparation method has theadvantages that the preparation method is simple and effective, the catalyst is easy to recycle and repeatedly use, the glucose with wide source and low cost is used as the reaction raw material, theeconomic benefit is high, and the good industrial application prospect is realized.
Owner:KUNMING UNIV OF SCI & TECH

Attapulgite-reinforced resin solid acid catalyst and preparation method thereof

The invention discloses a novel attapulgite-reinforced resin catalyst and a preparation method thereof. The novel solid acid catalyst is prepared by suspension polymerization by using attapulgite as an independent dispersing agent. The preparation method comprises the following steps: modifying attapulgite by using a silane coupling agent until the surface has appropriate hydrophilicity / hydrophobicity; synthesizing attapulgite / polystyrene microspheres by using the modified attapulgite as a dispersing agent; and finally, sulfonating by concentrated sulfuric acid to obtain the attapulgite-reinforced resin solid acid catalyst. The structure of the catalyst is determined by Fourier-infrared spectrum and a scanning electron microscope. In the lactic acid-butanol reaction, compared with the Amberlyst-15, the catalyst disclosed by the invention has better properties, stable structure and excellent anti-swelling property.
Owner:NANJING UNIV OF TECH

Synthesis method of high-4,4'-isomer-content bisphenol F

The invention discloses a synthesis method of high-4,4'-isomer-content bisphenol F, which comprises the following step: by using phenol and formaldehyde as raw materials, synthesizing bisphenol F by a two-step process by using Amberlyst-36 and Amberlyst-15 cation exchange resins as catalysts, wherein the mass percent of the 4,4'-isomer bisphenol F is up to 60% or above, and the mass yield of the bisphenol F is up to 90% or above. The catalysts are commercial cation exchange resins, can be easily purchased, separated and recovered, and are recyclable. The method has the advantages of low reaction temperature, short reaction time and no corrosiveness to equipment, is suitable for continuous production of tubular reactors, and has favorable industrial application prospects.
Owner:XIANGTAN UNIV

Method for preparing aniline green artificial antigens

The invention provides a method for preparing aniline green artificial antigens. The method includes steps of firstly, preparing and detecting haptens, and to be more specific, synthesizing the aniline green haptens from N, N-dimethylaniline and benzaldehyde derivatives by the aid of Amberlyst 15 resin under certain conditions; secondly, preparing and detecting artificial antigens, to be more specific, respectively coupling the obtained haptens and bovine gamma globulin (BGG) by the aid of active ester and diazotization processes and preparing the aniline green artificial antigens which are corresponding complete antigens formed by aniline green-bovine gamma globulin. The Amberlyst 15 resin is used as a catalyst. The method has the advantages that animal immunization can be carried out on the aniline green artificial antigens to obtain corresponding aniline green antibodies, the method can be used for researching diversified aniline green immunoassay processes, and convenient, quick and accurate ways can be provided for aniline detection.
Owner:HANGZHOU LAIHE BIOTECH CO LTD

Method for directly preparing alkyl levulinate from furfural

The invention discloses a method for directly preparing alkyl levulinate from furfural. The method is characterized in that the furfural is used as raw materials; low-grade alkanol is used as a reaction medium; a combination of a supported molecular sieve ZrO2 / MCM and ion exchange resin Amberlyst-15 is used as a catalyst; reaction is performed for 8 to 24h at 130 to 150 DEG C; an alkyl levulinateproduct with the yield reaching up to 85.3 percent can be obtained. In the process, the used catalyst system is cheap and can be easily obtained; the catalyst can be easily separated, recovered and repeatedly used; the one-step synthetic process is simple; the equipment is simplified; the reaction conditions are mild; the additional addition of hydrogen gas is not needed; the safe and environment-friendly effects are achieved; the conversion efficiency is high; the target product yield is high; good industrial application prospects are realized.
Owner:KUNMING UNIV OF SCI & TECH

Preparation of functionalized castor oil derivatives using solid acid and base catalysts

This invention relates to the development of processes for the preparation of functionalized castor oil derivatives namely ring-opened glyceryl ricinoleates, epoxy alkyl ricinoleates and ring-opened alkyl ricinoleates with tailorable properties from epoxidized castor oil as raw material using heterogeneous acid and base catalysts. More particularly, the invention employs two reaction chemistries namely ring-opening and transesterification using Amberlyst 15 as solid acid catalyst for the former and oxides derived from CaAl layered double hydroxide (CaAl-LDH) as solid base catalyst for the latter and combinations thereof. Furthermore, both the catalysts are reusable and the products are easily separable after the reaction by simple physical processes.
Owner:COUNCIL OF SCI & IND RES

Synthetic method of diallyl diethylene glycol carbonate

The invention belongs to the technical field of synthesis of diallyl diethylene glycol carbonate, and particularly relates to a synthetic method of diallyl diethylene glycol carbonate. The synthetic method comprises the following steps of: (1) adding diethylene glycol, allyl alcohol, dimethyl carbonate and catalyst ion exchange resin Amberlyst-15 into a reaction still, reacting the dimethyl carbonate with the allyl alcohol to generate diallycarbonate and methanol, carrying out an ester exchange reaction on the diallycarbonate and the diethylene glycol at 50-140 degree centigrade, reflowing and thermally insulating for 2-3 hours; and (2) distilling the reaction liquid in the step (1), recovering methanol at 65-90 DEG C, recovering allyl alcohol and diallycarbonate at 95-140 DEG C, reducing to the room temperature of the catalyst-containing mixed liquor, filtering and separating the catalyst ion exchange resin Amberlyst-15 to obtain required products. The synthetic method of diallyl diethylene glycol carbonate disclosed by the invention has the advantages of simple method, heat-resisting catalyst and high purity of the obtained products, and is capable of saving the production cost.
Owner:山东鲁源化工科技有限公司

Synthesis process of N-sustituent-4-piperidyl alcohol

The synthesis process of preparing N-substituent-4-piperidyl alcohol includes the following steps: 1. adding primary amine into ethyl acrylate to react to obtain the secondary addition product; 2. adding cyclizing agent into the secondary addition product and adding concentrated hydrochloric acid after finishing cyclization to obtain N-substituent-4-piperidone hydrochloride; 3. reducing N-substituent-4-piperidone hydrochloride with NaBH4-Amberlyst-15(H+) system and regulating pH value to extract N-substituent-4-piperidyl alcohol; and 4. recovering and treating resin for reuse. The present invention has wide raw material resource, mild reaction condition, simple operation, low production cost, high yields in different steps, and excellent industrial application foreground.
Owner:SOUTHEAST UNIV

Synthesis process of N-sustituent-4-piperidyl alcohol

The synthesis process of preparing N-substituent-4-piperidyl alcohol includes the following steps: 1. adding primary amine into ethyl acrylate to react to obtain the secondary addition product; 2. adding cyclizing agent into the secondary addition product and adding concentrated hydrochloric acid after finishing cyclization to obtain N-substituent-4-piperidone hydrochloride; 3. reducing N-substituent-4-piperidone hydrochloride with NaBH4-Amberlyst-15(H+) system and regulating pH value to extract N-substituent-4-piperidyl alcohol; and 4. recovering and treating resin for reuse. The present invention has wide raw material resource, mild reaction condition, simple operation, low production cost, high yields in different steps, and excellent industrial application foreground.
Owner:SOUTHEAST UNIV

Method for reinforcing oleophobic property of catalyst surface

The invention discloses an oleophobic property reinforcing method of catalyst surface, which comprises the following steps: coating certain acid catalyst with oleophobic property such as Teflonx-{[(HSiW) / (SiO2)]y)(1-x), Teflonx / Amberlyst-15 and Teflonx / Amberlyst-35; detecting the finishing and finished touch corner of solid acid surface and soybean oil drip through droplet shape analyzer.
Owner:CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI

Method for synthesizing diethoxymethane from dimethoxymethane and ethanol

The invention provides a method for synthesizing diethoxymethane from dimethoxymethane and ethanol, relating to a method for preparing methane. The method comprises the following step: by using dimethoxymethane and ethanol as raw materials, reacting at 0-160 DEG C under the reaction pressure of 0.1-10.0 MPa by using a liquid acid and a supported liquid acid as catalysts to generate diethoxymethane at high selectivity. The resin catalyst is one or more of KAD302, KC107, NKC-9, DA-330, D009B, Amberlyst-15 and D072H containing sulfonic acid functional group. The reaction temperature is 0-160 DEG C, and the reaction pressure is 0.1-10.0 MPa. The filling gas is inert gas which is argon, helium, carbon dioxide or N2 mixture or a gas mixture thereof. The method has the advantages of single product and high selectivity, and has favorable application prospects. The required raw materials are cheap and accessible, and the whole process is simple to operate and can not generate any environment-polluting chemical substance. Thus, the method belongs to an environment-friendly technical route.
Owner:SHENYANG INSTITUTE OF CHEMICAL TECHNOLOGY

Process for one pot conversion of artemisinin into artelinic acid

The present invention relates to an improved process for one pot conversion of artemisinin into artelinic acid, which reduces the three step (three pot) conversion of artemisinin to artelinic acid in one step (one pot). The process of preparation of artelinic acid involves stirring of artemisinin with sodium borohydride, catalyst, polyhydroxy compound or chlorotrimethylsilane or amberlyst-15 resin and methyl p-(hydroxymethyl) benzoate, filtration of undissolved, unwanted reaction products and finally stirring of the filtrate with alcoholic or aqueous alkali hydroxide.
Owner:COUNCIL OF SCI & IND RES

Oxapium iodide preparation method

The invention discloses an oxapium iodide preparation method. The method comprises the steps of S1, preparing 2-phenyl-2-hexamethylene-4-methanol-1,3-dioxolane, S2, preparing 2-phenyl-2-hexamethylene-4-piperidinemethyl-1, 3-dioxolane, and S3, preparing the oxapium iodide. The step S1 comprises the steps of mixing uniformly cyclohexyl phenyl ketone, glycerol, Amberlyst-15 exchange resin and allochroic silicagel, heating, maintaining the temperature, stirring, filtering, taking the filtered solution, adding saturated sodium hydrogen carbonate aqueous solution for washing, keeping static, taking organic layer, drying, releasing pressure, distilling to acquire material A, purifying material A, drying to acquire 2-phenyl-2-hexamethylene-4-methanol-1, 3-dioxolane. The method has the advantages of being mild in reaction condition, simple in operation, suitable for industrialized production, low in material toxicity, easy and cheap for material access, low in cost and good in comprehensive yield rate.
Owner:HEFEI PINGGUANG PHARMA

Preparation of quinoxaline derivatives

The invention discloses a preparation method of a quinoxaline derivative. The method is characterized by condensing an o-diamino compound with an o-dicarbonyl compound in a polar solvent in the presence of catalyst Amberlyst-15 or NKC-9 dry hydrogen catalyzed resin Styrene-DVB to prepare the quinoxaline derivative. The preparation method takes ordinary tap water instead of a toxic organic solventas the solvent for a condensation reaction to obtain the quinoxaline derivative with high yield and high content. The catalyst can be recovered and can be reused for at least three times in a condition of no loss of the catalytic activity, thus effectively reducing the production cost. The preparation method of the quinoxaline derivative has the advantages of simple process operation, no environment pollution, and is fit for large-scale industrialized production.
Owner:TIANJIN NORMAL UNIVERSITY

Method for preparing dibutoxymethane from dimethoxymethane and n-butyl alcohol

The invention provides a method for preparing dibutoxymethane from dimethoxymethane and n-butyl alcohol and relates to a method for preparing dibutoxymethane. The method comprises steps as follows: dimethoxymethane and n-butyl alcohol which serve as raw materials are subjected to a reaction in the presence of catalysts, namely, liquid acid and supported liquid acid, at the reaction temperature of 0-160 DEG C under the reaction pressure of 0.1-10.0 MPa, and dibutoxymethane is produced in a high-selective manner; a resin catalyst is one or more of KAD302, KC107, NKC-9, DA-330, D009B, Amberlyst-15, D072H and the like which contain sulfonic acid functional groups; the reaction temperature is 0-160 DEG C and the reaction pressure is 0.1-10.0 MPa. According to the method, a single product is produced, the selectivity is high, required raw materials are low in price and easy to obtain, the operation is simple in the whole procedure, no chemical substances polluting the environment are produced, and the method is an environment-friendly technological process.
Owner:SHENYANG INSTITUTE OF CHEMICAL TECHNOLOGY

Conversion of Wood Based Hemicellulose Prehydrolysate into Succinic Acid Using a Heterogeneous Acid Catalayst in a Biphasic System

A novel approach for the conversion of biomass based hemicellulose prehydrolysate to high value succinic acid has been investigated using a heterogeneous acid catalyst, Amberlyst 15 and hydrogen peroxide. A vital intermediate in this process, furfural, was oxidized in a biphasic system to produce succinic acid. Production of furfural in good yields is a limiting step in such processes for a number of reasons. Among the organic solvents evaluated, toluene was found to be an ideal solvent for furfural extraction and facilitated the conversion of furfural to succinic acid. Simultaneous extraction of furfural into the organic solvent as it is produced, increased the overall yield. It was observed that the developed method resulted in a succinic acid yield of 49% from the furfural obtained from hemicellulose prehydrolysate. It was found that 50 mg of Amberlyst 15 per mmole of furfural resulted in 100% FA conversion in less time.
Owner:LAKEHEAD UNIVERSITY

Preparation of functionalized castor oil derivatives using solid acid and base catalysts

This invention relates to the development of processes for the preparation of functionalized castor oil derivatives namely ring-opened glyceryl ricinoleates, epoxy alkyl ricinoleates and ring-opened alkyl ricinoleates with tailorable properties from epoxidized castor oil as raw material using heterogeneous acid and base catalysts. More particularly, the invention employs two reaction chemistries namely ring-opening and transesterification using Amberlyst 15 as solid acid catalyst for the former and oxides derived from CaAl layered double hydroxide (CaAl-LDH) as solid base catalyst for the latter and combinations thereof. Furthermore, both the catalysts are reusable and the products are easily separable after the reaction by simple physical processes.
Owner:COUNCIL OF SCI & IND RES

A kind of synthetic method of high 4,4'-isomer content bisphenol f

The invention discloses a synthesis method of high-4,4'-isomer-content bisphenol F, which comprises the following step: by using phenol and formaldehyde as raw materials, synthesizing bisphenol F by a two-step process by using Amberlyst-36 and Amberlyst-15 cation exchange resins as catalysts, wherein the mass percent of the 4,4'-isomer bisphenol F is up to 60% or above, and the mass yield of the bisphenol F is up to 90% or above. The catalysts are commercial cation exchange resins, can be easily purchased, separated and recovered, and are recyclable. The method has the advantages of low reaction temperature, short reaction time and no corrosiveness to equipment, is suitable for continuous production of tubular reactors, and has favorable industrial application prospects.
Owner:XIANGTAN UNIV

A kind of method that solid acid catalysis high yield prepares levulinic acid ester

The invention discloses a high-yield levulinic acid ester preparation method under catalysis of solid acid and belongs to the field of organic synthesize. The method comprises the following steps: uniformly mixing 1 part of sugar, 10-100 parts of alcohol, 0.01-0.2 part of acid B and 0.1-1 part of acid L, and performing reaction under the temperature of 130-190 DEG C for 1-20 h to obtain a levulinic acid methyl ester solution, wherein the acid L is stanniferous molecular sieve, and the acid B is SBA-15-SO3H, Carbon-SO3H or Amberlyst-15. According to the method, the carbohydrate is low in cost and easy to obtain; with the acid B and acid L which can be used repeatedly, the catalysis effect basically remains the same; the levulinic acid ester compound prepared in one step can be widely applied to industries of food additives, essence spices, chemical reaction intermediates, gasoline, diesel-dopes and the like.
Owner:GUANGZHOU CHEM CO LTD CHINESE ACADEMY OF SCI
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