Synthetic preparation method of wintergreen oil

A technology of wintergreen oil and synthetic reaction, which is applied in the preparation of organic compounds, carboxylic acid ester preparation, chemical instruments and methods, etc., can solve the problems of complex catalyst preparation process, complex reaction follow-up treatment, complex synthetic reaction, etc., and shorten the production process. Effects of cycle, increasing difficulty, and simple reaction process

Active Publication Date: 2019-03-12
江西省隆南药化有限公司
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although this method overcomes some defects of the traditional concentrated sulfuric acid catalytic method, it still has the disadvantages of using p-toluenesulfonic acid as a catalyst, which is expensive and difficult to recycle; Preparation process of methyl salicylate", the preparation process adopts sol-gel technology to prepare TiO2 composite photocatalyst, instead of traditional concentrated sulfuric acid catalyst
Although this process overcomes some defects of the traditional concentrated sulfuric acid catalysis method, there are disadvantages such as the use of TiO2 composite photocatalyst, the preparation process of the catalyst is complicated, the whole synthesis reaction is complicated, the practicability is poor, and the follow-up treatment of the reaction is complicated; another example: Publication No. The patent name of CN105622403A is "a method for the synthesis and preparation of high-quality methyl salicylate". The synthesis method uses a new catalyst to replace the original concentrated sulfuric acid catalyst. and additives, wherein the base material is silicon dioxide, diatomaceous earth and aluminum oxide, and the polysaccharide is one or more of polyacetylglucosamine, galactose and polyfructose, and the sulfide It is one or both of potassium hydrogen sulfate and copper sulfate, and the auxiliary agent is one or both of polyvinyl alcohol and polysorbate
Although this synthesis method overcomes some defects of the traditional concentrated sulfuric acid catalytic method, there are still shortcomings such as complex preparation process of the catalyst, poor practicability, and complicated post-reaction treatment.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Embodiment 1: use methyl formate as catalyst-small test to prepare wintergreen oil

[0023] According to the molar ratio of 2:1:0.2, accurately weigh 128.16g of methanol, 276.24g of salicylic acid, and 24.02g of methyl formate, and put them into the high-pressure reactor in turn, control the reaction temperature at 150°C, and the pressure at 0.9MPa. Under the reaction 6h. After the reaction is completed, the temperature is lowered to normal temperature, the reaction solution is transferred to a three-necked flask, and the 25 cm packed column (with ceramic Pall rings as the filler) is subjected to rough steaming under normal pressure to collect methanol fractions at 30-66°C. After the collection is completed, the vacuum pressure is controlled at -0.09 ~ -0.10MPa, and the fraction at 75-80°C is collected until no liquid evaporates. 298.45 g of finished wintergreen oil was obtained, the product purity was 99.6%, and the conversion rate was 97.78%.

Embodiment 2

[0024] Embodiment 2: make catalyzer-small test preparation wintergreen oil with methyl acetate:

[0025] Accurately weigh 128.16g of methanol, 276.24g of salicylic acid, and 29.63g of methyl acetate according to the molar ratio of 2:1:0.2, and put them into a high-pressure reactor in sequence. The reaction was stirred for 6h. After the reaction was completed, the temperature was lowered to normal temperature, the reaction solution was transferred to a three-necked flask, and the 25cm packed column (with ceramic Pall ring as the filler) was subjected to rough steaming under normal pressure to collect fractions at 50-66°C. After the collection is completed, the vacuum pressure is controlled at -0.09 ~ -0.10MPa, and the fraction at 75-80°C is collected until no liquid evaporates. Obtain 272.01g of finished wintergreen oil, product purity is 99.6%, conversion rate is 89.12%.

Embodiment 3

[0026] Embodiment 3: use methyl butyrate as catalyst-small test to prepare wintergreen oil:

[0027] Accurately weigh 128.16g of methanol, 276.24g of salicylic acid, and 40.85g of methyl butyrate according to the molar ratio of 2:1:0.2, and put them into a high-pressure reactor in sequence. Control the reaction temperature at 150°C and the pressure at 0.9MPa. The reaction was stirred for 6h. After the reaction was completed, the temperature was lowered to normal temperature, the reaction solution was transferred to a three-necked flask, and the 25 cm packed column (with glass Pall ring as the filler) was subjected to rough steaming under normal pressure to collect fractions at 50-66°C. After the collection is completed, the vacuum pressure is controlled at -0.09 ~ -0.10MPa, and the fraction at 75-80°C is collected until no liquid evaporates. Obtain 263.52g of finished wintergreen oil, the product purity is 99.5%, and conversion rate is 86.25%.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention relates to the field of chemical synthesis, and particularly discloses a synthetic preparation method of wintergreen oil. The synthetic preparation method comprises the following steps:(1) methanol, salicylic acid and methyl carboxylate are sequentially put into a reaction kettle according to the molar ratio of (2 to 3):1:(0.1 to 0.3); (2) a synthetic reaction is generated under theconditions of heating and pressurization, and a mixed solution A containing the wintergreen oil is obtained; and (3) the mixed solution A is distilled and separated to obtain the wintergreen oil. According to the method, the defects of a traditional concentrated sulfuric acid catalytic method are overcome, and the methyl carboxylate serves as a catalyst, so that the beneficial effects that raw materials are easy to obtain, the reaction flow is simple, the catalyst can be removed only through simple distillation, subsequent treatment is easy, and the prepared wintergreen oil is large in product purity and high in conversion rate are achieved.

Description

technical field [0001] The invention belongs to the field of chemical synthesis, and in particular relates to a synthetic preparation method of wintergreen oil. Background technique [0002] Wintergreen oil has a wintergreen aroma and is also known as Methyl Salicylate. It exists widely in nature and is the main component of wintergreen and Xiaodang medicinal oil. It is now widely used as a solvent, preservative, and fixative in fine chemical industry, and also as a spice for beverages, food, toothpaste, cosmetics, etc., as well as for the production of analgesics, insecticides, polishes, inks, and Fiber dyeing aids, etc., and its anti-inflammatory, analgesic, bactericidal effects and ability to penetrate the skin are widely used in the pharmaceutical industry. [0003] The traditional synthetic method of wintergreen oil is mainly esterification. This method takes salicylic acid and methanol as raw materials, and carries out esterification synthesis reaction under the cata...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C07C67/08C07C69/84
CPCC07C67/08C07C69/84
Inventor 万贵生刘遗松赖神风钟庆瑜梁毅
Owner 江西省隆南药化有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products