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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244405Generated: October 27, 2026

Hydrochloric Acid → Methyl 5-bromo-2-methyl-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/2244405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant5-Bromo-2-methyl-1,3-thiazole-4-carboxylic acidHCID 45117584—
SolventDiethyl EtherHCID 3283—
ProductMethyl 5-bromo-2-methyl-1,3-thiazole-4-carboxylateHCID 1642715582%

Reaction Steps

A solution of 5-bromo-2-methyl-thiazole-4-carboxylic acid (1.50 g, 6.75 mmol) in methanol (80.00 ml) was treated with a saturated solution of HCl in ether (3.00 ml). The reaction mixture was heated at reflux for 3 h then the volatiles were removed. The residue was purified by flash chromatography (methylene chloride/methanol) yielding 5-bromo-2-methyl-thiazole-4-carboxylic acid methyl ester (1.30 g, 82%) as a white solid, MS (ISP): m/e=235.9, 237.9 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678815B2
Source datasetuspto-grants-2010_03
ORD IDord-157b3d133e4446e08515daba6cc1b04c
Source noteuspto-grants-2010_03