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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351510Generated: October 31, 2026

Sodium Hydroxide → (2S)-2-Ethoxy-3-(4-hydroxyphenyl)propanoic acid

https://huagongshe.com/reaction/351510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-ethoxy-3-(4-hydroxyphenyl)propanoateHCID 11791243—
SolventPhosphateHCID 1061—
Product(2S)-2-Ethoxy-3-(4-hydroxyphenyl)propanoic acidHCID 983720740.8%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743608B2
Source datasetuspto-grants-2004_06
ORD IDord-b42e0c1f7ce640a2ae0a02c94c2e8b44
Source noteuspto-grants-2004_06