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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638415Generated: October 30, 2026

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

https://huagongshe.com/reaction/638415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(2-t-pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylateHCID 19978748—
ReactantHCID 178473043HCID 178473043—
SolventWaterHCID 962—
Product(2-t-Pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylic acidHCID 19978737—

Reaction Steps

A mixture of ethyl 2-(2-tert-pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylate, which can be represented as ethyl 2-(2-tert-pentyloxycarbonylimino-2,3-dihydro-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, which can be represented as 2-(2-tert-pentyloxycarbonylimino-2,3-dihydro-1,3-thiazol-4-yl)glyoxylic acid, (1.75 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04560765
Source datasetuspto-grants-1985_12
ORD IDord-54f3f964cb4a48d9b6ec94fba882072a
Source noteuspto-grants-1985_12