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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446409Generated: October 29, 2026

Ethyl bromopyruvate → Ethyl 2-ethyl-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/446409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantPropanethioamideHCID 2760628—
Reactant2-(2-Chloro-5-(hydroxymethyl)phenyl)ethanolHCID 57989337—
SolventEthanolHCID 702—
ProductEthyl 2-ethyl-1,3-thiazole-4-carboxylateHCID 15056276—

Reaction Steps

Ethyl 3-bromo-2-oxopropanoate (24.7 mL) was added dropwise over 10 min to a solution of propanethioamide [Carboxylic Acid 1, step a] (15.8 g) in ethanol (150 mL) at 0-10° C. under nitrogen. When the addition was complete the mixture was stirred at ambient temperature for 18 hours. The mixture was concentrated in vacuo, the residue diluted with water and extracted into ethyl acetate (×3). The combined extracts were washed with brine, dried over magnesium sulfate, filtered and the solvent removed. The crude product was purified by flash silica chromatography, elution gradient 10, 15 and 20% ethyl acetate in isohexane. Fractions containing the product were evaporated to dryness to afford the subtitled compound as a pale green solid. Yield 16.0 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476265B2
Source datasetuspto-grants-2013_07
ORD IDord-6bf56635758548ac98369446656d35ab
Source noteuspto-grants-2013_07