Method for preparing long-chain dicarboxylic dialkyl ester
A technology for dialkyl chain dicarboxylic acid and long chain dicarboxylic acid, which is applied in the field of preparing dialkyl esters, can solve the problems of reducing the reaction rate of esterification, low reaction temperature, and many operation steps, and achieves improved esterification. The effect of reaction rate, shortened operation cycle, and reduced production cost
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0035] Add 60g of refined dodecanedioic acid, 480g of 2-ethylhexanol and 22g of "DNW" cation exchange resin produced by Dandong No. The esterification reaction was carried out at this temperature, and water was continuously evaporated during the reaction process, which was collected in a receiving bottle and reacted for 3.5 hours. At this time, no more water was evaporated, and the reaction was terminated. Reaction liquid is distilled under reduced pressure, reclaims unreacted alcohol, then with the NaHCO of 50ml 2N 3 The obtained crude ester was washed with solution (preheated to 60°C), and then washed with hot water at 60°C until neutral. The residual moisture in the crude ester was evaporated under a vacuum degree of 50 kPa to obtain 106.3 g of bis(2-ethylhexyl) dodecanedioate, and the esterification recovery rate was 94.6 wt%.
Embodiment 2
[0037] Add 70g of pentadecanedioic acid with bacteria (pentadecanedioic acid content 89.0%), 300g of isotridecanol and 4.2g of Beijing Guanghua Wood Factory "GH-88" powdered activated carbon into 1000ml with reflux condenser In a three-necked flask, heated to 80°C under stirring, decolorized and adsorbed for 1 hour, and the stirring speed was 80r / min. Then filter while it is hot to obtain the alcohol solution of dicarboxylic acid, add the filtrate to a 500ml three-neck flask with a distillation receiving system, and add 28g of "DNW" cation exchange resin produced by Dandong No. 3 Chemical Factory, and heat the reaction solution to 130°C under stirring , Receive the water evaporated in the reaction process in the receiving bottle, and stop the reaction until no water distills out, and the reaction time is 3.2h. The rest of the steps and conditions were the same as in Example 1, and 136.2 g of diisotridecyl pentadecanedioate was obtained, with an esterification recovery rate of 93...
Embodiment 3
[0039] Add 60g of refined tridecanedioic acid, 350g of isodecyl alcohol, 2g of 1,2-butanediol and 50g of "DNW" cation exchange resin produced by Dandong No. The reaction solution was heated to 100°C for esterification reaction, and the reaction was stopped when no water evaporated, and the reaction time was 4.6 hours. Then reclaim unreacted isodecyl alcohol according to the method of Example 1, alkali washing, water washing, dehydration, make tridecanedioic acid diisodecyl-tridecanedioic acid butanediol complex ester 118.2g, esterification recovery Rate 93.8wt%.
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com