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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988762Generated: November 3, 2026

Butanoic acid, 4-chloro-4-oxo-, ethyl ester → Ethyl 4-(2-thiazolyl)-4-oxobutyrate

https://huagongshe.com/reaction/1988762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanoic acid, 4-chloro-4-oxo-, ethyl esterHCID 84648—
ReactantSodium BicarbonateHCID 516892—
Reactant2-TrimethylsilylthiazoleHCID 588453—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-(2-thiazolyl)-4-oxobutyrateHCID 68499389—

Reaction Steps

To a stirred solution of 2-trimethylsilanyl-thiazole (2.6 g, 16.53 mmol) in DCM (30 mL) is added a solution of 3-chlorocarbonyl-propionic acid ethyl ester (5.4 g, 32.81 mmol) in DCM (10 mL). The mixture is stirred overnight at room temperature. To the mixture is added 5% NaHCO3 (30 mL) and mixture is stirred at room temperature for 20 minutes. The organic layer is separated and the aqueous lay is extracted with DCM (2×50 mL). The combined organic layers are dried and the solvent removed. The residue is separated by column (methylene chloride) to give 4-oxo-4-thiazol-2-yl-butyric acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642267B2
Source datasetuspto-grants-2010_01
ORD IDord-37e34f4a12de4635b0f7fa48efd0416a
Source noteuspto-grants-2010_01