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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517539Generated: October 26, 2026

Ethyl thiooxamate → Ethyl 5-(3-bromobenzyl)-4-methylthiazole-2-carboxylate

https://huagongshe.com/reaction/517539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl thiooxamateHCID 2733398—
Reactant3-Bromo-4-(3-bromophenyl)butan-2-oneHCID 62393918—
SolventEthanolHCID 702—
ProductEthyl 5-(3-bromobenzyl)-4-methylthiazole-2-carboxylateHCID 8671148042.1%

Reaction Steps

A mixture of 3-bromo-4-(3-bromophenyl)butan-2-one (1.8 g, 5.9 mmol) and ethyl 2-amino-2-thioxoacetate (745 mg, 5.6 mmol) in EtOH (20 mL) was refluxed overnight. The solvent was removed and the residue was purified by silica gel column chromatography (EtOAc:Petroleum ether=1:5) to afford ethyl 5-(3-bromobenzyl)-4-methylthiazole-2-carboxylate as a light yellow solid (800 mg, 42.1%). MS (ES+) C14H14BrNO2S requires: 339, 341 found: 340[M+H]+, 342 [M+2+H]+(1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115120B2
Source datasetuspto-grants-2015_08
ORD IDord-b9e1a5fcec0d4727a7ff2f29d26f66be
Source noteuspto-grants-2015_08