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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390544Generated: October 30, 2026

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

https://huagongshe.com/reaction/2390544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantPropanethioamideHCID 2760628—
SolventEthanolHCID 702—
ProductEthyl 2-ethyl-1,3-thiazole-4-carboxylateHCID 15056276—

Reaction Steps

Ethyl 3-bromo-2-oxopropanoate (4.10 mL, 32.67 mmol) was added dropwise over 10 min to a stirred solution of propanethioamide (3 g, 33.65 mmol) in ethanol (40 mL) cooled in an ice bath. After 16 h the reaction mixture was evaporated in vacuo. Purification was by silica gel chromatography eluting with EtOAc:iso-hexanes, 1:3 to give the sub-title compound as a yellow oil. Yield: 2.78 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273774B2
Source datasetuspto-grants-2012_09
ORD IDord-a2016dbc73054a85a204793783074cae
Source noteuspto-grants-2012_09