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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372186Generated: October 25, 2026

Sodium Hydroxide → 2-Bromothiazole-5-carboxylic acid

https://huagongshe.com/reaction/372186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-bromothiazole-5-carboxylateHCID 2773502—
SolventMethanolHCID 887—
Product2-Bromothiazole-5-carboxylic acidHCID 2763210—

Reaction Steps

A mixture containing 10 g. of 2-bromo-5-methoxycarbonylthiazole, 100 ml. of 10% aqueous sodium hydroxide and 200 ml. of methanol is stirred at 0° C for 5 minutes. The methanol is distilled off in vacuo and the resulting concentrate extracted twice with ethyl acetate. The remaining aqueous phase is acidified by the careful addition of dilute aqueous hydrochloric acid resulting in the formation of a precipitate which is then recovered by filtration and dried under vacuum yielding 2-bromo-5-carboxythiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04089865
Source datasetuspto-grants-1978_05
ORD IDord-88dc2156b4c1436ba9bdcaf5319c1528
Source noteuspto-grants-1978_05