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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265635Generated: October 30, 2026

Methanol → 3-(5-Hydroxymethyl-thiazol-4-yl)-benzoic acid methyl ester

https://huagongshe.com/reaction/1265635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium AcetateHCID 517044—
ReactantSodium MethoxideHCID 10942334—
Reactant3-(5-Bromomethyl-thiazol-4-yl)-benzoic acid methyl esterHCID 69687702—
SolventDimethylformamideHCID 6228—
Product3-(5-Hydroxymethyl-thiazol-4-yl)-benzoic acid methyl esterHCID 69688643—

Reaction Steps

3-(5-Bromomethyl-thiazol-4-yl)-benzoic acid methyl ester was stirred in DMF (10 mL) together with KOAc (1.52 g) at 20° C. for 30 min. MeOH (20 mL) and NaOMe (0.84 g) were added and stirring was continued at 50° C. for 30 min. The mixture was partitioned between AcOEt and brine and the organic layer was dried and evaporated. The residual oil was chromatographed on silica gel using AcOEt/hexane (1:2) as eluent to give 3-(5-hydroxymethyl-thiazol-4-yl)-benzoic acid methyl ester (1.43 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544985B2
Source datasetuspto-grants-2003_04
ORD IDord-59e4add3a39c41a68be664d6119e8a98
Source noteuspto-grants-2003_04