Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864548Generated: October 26, 2026

Methanol → methyl 2(S)-ethoxy-3-[4-(2-methylaminothiazol-5-yl)phenyl]propanoate

https://huagongshe.com/reaction/1864548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant2(S)-Ethoxy-3-[4-(2-methylaminothiazol-5-yl)phenyl]propanoic acidHCID 86606238—
CatalystSulfuric AcidHCID 1118—
SolventWaterHCID 962—
Productmethyl 2(S)-ethoxy-3-[4-(2-methylaminothiazol-5-yl)phenyl]propanoateHCID 8660623967%

Reaction Steps

0.5 g (1.6 mmol) of 2(S)-ethoxy-3-[4-(2-methylaminothiazol-5-yl)phenyl]propanoic acid in 10 ml of methanol and a few drops of sulfuric acid is heated at 60° C. for 2 hours. The reaction medium is cooled, diluted with water, neutralized to pH 7 with aqueous 1M sodium hydroxide solution and then extracted with ethyl acetate. The organic phase is washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with a 50/50 heptane/ethyl acetate mixture. 0.34 g (67%) of methyl 2(S)-ethoxy-3-[4-(2-methylaminothiazol-5-yl)phenyl]propanoate is obtained in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625914B2
Source datasetuspto-grants-2009_12
ORD IDord-4638bf797eed44e5ae3f4daf4e45c44d
Source noteuspto-grants-2009_12