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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648397Generated: October 29, 2026

Ethanol → (2-t-Pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylic acid

https://huagongshe.com/reaction/648397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(2-t-pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylateHCID 19978748—
SolventWaterHCID 962—
Product(2-t-Pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylic acidHCID 1997873768.6%

Reaction Steps

A mixture of ethyl 2-(2-tert-pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylate (2.8 g.) and ethanol (10 ml.) was mixed with a solution of sodium hydroxide (0.54 g.) in water (20 ml.), and the mixture was stirred for 1 hour at room temperature. After the reaction, a small amount of ethanol was distilled off. The remaining reaction mixture was washed with diethyl ether and then the aqueous layer was separated therefrom. To the aqueous layer was added ethyl acetate, and the mixture was adjusted to pH 1 to 2 with 10% hydrochloric acid and then the ethyl acetate layer was separated therefrom. The ethyl acetate layer was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and then treated with activated charcoal. The solvent was distilled off from the ethyl acetate layer to give yellow brown powder of 2-(2-tert-pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylic acid (1.75 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04411898
Source datasetuspto-grants-1983_10
ORD IDord-58ed63f24b004e66a6151ce6cbb1b9d2
Source noteuspto-grants-1983_10