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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708947Generated: November 2, 2026

Ethyl 2-chloroacetoacetate → Ethyl 2-(4-methoxyphenyl)-4-methyl-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1708947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloroacetoacetateHCID 11858—
Reactant4-MethoxybenzenecarbothioamideHCID 736827—
SolventEthanolHCID 702—
ProductEthyl 2-(4-methoxyphenyl)-4-methyl-1,3-thiazole-5-carboxylateHCID 754095276.3%

Reaction Steps

To a solution of p-methoxythiobenzamide (3 g, 17.95 mmol) dissolved in dry ethanol (180 ml) was added ethyl 2-chloroacetoacetate (1.28 ml, 8.98 mmol), and the mixture was heated under reflux for 1.5 hours. After the reaction was completed, the solvent was distilled off from the reaction mixture. Then the residue was treated with water, made weak alkali (pH=8) with saturated aqueous sodium carbonates, and extracted with ethyl acetate. The organic phase was washed with saturated saline and dried over anhydrous sodium sulfate. After removing the solvent by distillation, the residue was dissolved in chloroform (insoluble solids being filtered off) and applied on silica gel column (developing solvent:n-hexane:ethyl acetate=85:15). After discarding the first fraction (impurities), the second colorless fraction was pooled and concentrated to give 1.9 g of ethyl 2-(4-methoxyphenyl)-4-methyl-5-thiazolecarboxylate as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04946855
Source datasetuspto-grants-1990_08
ORD IDord-7b76aed4ba2a4ddc92da432587be5eb7
Source noteuspto-grants-1990_08