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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058350Generated: November 3, 2026

Ethyl 2-chloroacetoacetate → Ethyl 2-ethyl-4-methyl-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1058350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloroacetoacetateHCID 11858—
ReactantPropanethioamideHCID 2760628—
SolventEthanolHCID 702—
ProductEthyl 2-ethyl-4-methyl-1,3-thiazole-5-carboxylateHCID 2356069381.5%

Reaction Steps

A solution of ethyl 2-chloroacetoacetate (2.00 g, 10.04 mmol) and thiopropionamide (1.00 g, 11.22 mmol) in ethanol (100 mL) was heated at reflux overnight. The solvent was evaporated and dichloromethane (100 mL) added. The solution was washed with water (2×100 mL) and brine (100 mL), dried (MgSO4), filtered, evaporated and the concentrate was chromatographed over silica gel (10% ethyl acetate/hexanes) to give 2-ethyl-4-methylthiazole-5-carboxylic acid ethyl ester (1.63 g, 81% yield) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515124B2
Source datasetuspto-grants-2003_02
ORD IDord-b83915895e264ac5ae4bcc8fa8f3e220
Source noteuspto-grants-2003_02