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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663665Generated: October 30, 2026

Ethyl bromopyruvate → Ethyl 2-(cyanomethyl)-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1663665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
Reactant2-CyanoethanethioamideHCID 1416277—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(cyanomethyl)-1,3-thiazole-4-carboxylateHCID 80107626%

Reaction Steps

To a solution of ethyl 3-bromo-2-oxopropanate (21 g, 110 mmol) in N,N-dimethylformamide (50 mL) was added a solution of 2-cyanoethanethioamide (10 g, 100 mmol) in N,N-dimethylformamide (50 mL) under ice-cooling, and the reaction mixture was stirred at room temperature for 12 hr. The mixture was concentrated under reduced pressure, and the obtained residue was dissolved in ethyl acetate, and washed with 5% aqueous sodium hydrogencarbonate solution and saturated brine. The organic layer was dried over anhydrous sodium sulfate and filtrated. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=20/80→60/40) to give the title compound (5.1 g, 26%) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034812B2
Source datasetuspto-grants-2011_10
ORD IDord-5ad1b55cb1934ca18a27670a5d09af45
Source noteuspto-grants-2011_10