反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
Ethyl (2R/S) (+/−) 2-ethoxy-3-(4-hydroxyphenyl)propanoate (5 g) was added to an aqueous 0.1 M phosphate buffer pH 7 (10 ml). 100 mg of the lyophilised hydrolytic enzyme mixture from Aspergillus oryzae was added and the mixture was stirred for 18 hours at room temperature. During that time, the pH of the reaction mixture was kept constant at pH=6-8 by addition of NaOH. Most of the water was evaporated in vacuo. Methanol was added to the remaining slurry in order to stop the hydrolysis. The precipitate, which formed was filtered off and the methanol was evaporated in vacuo. The remaining oil was dissolved in water followed by extraction of unreacted ester with TMBE (CCE method 2: eeester=87%). The water phase was acidified to pH=3 and the acid extracted with TMBE. After drying over Na2SO4 and evaporation of the TMBE, 1.8 g (2S)-2-Ethoxy-3-(4-hydroxyphenyl)propanoic acid was obtained as an oil, which crystallized on standing (m.p.=105° C., CCE method 2: eeacid=>99%).
WORKUP
后处理
- addition100 mg of the lyophilised hydrolytic enzyme mixture from Aspergillus oryzae was added
- customMost of the water was evaporated in vacuo
- additionMethanol was added to the remaining slurry in order
- customthe hydrolysis
- customThe precipitate, which formed
- filtrationwas filtered off
- customthe methanol was evaporated in vacuo
- dissolutionThe remaining oil was dissolved in water
- extractionfollowed by extraction of unreacted ester with TMBE (CCE method 2: eeester=87%)
- extractionthe acid extracted with TMBE
- dry with materialAfter drying over Na2SO4 and evaporation of the TMBE