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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689404Generated: October 25, 2026

Ethyl bromopyruvate → 2-Methylpentane

https://huagongshe.com/reaction/1689404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantPentanethioamideHCID 12534254—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product2-MethylpentaneHCID 7892—
ProductEthyl 2-butyl-1,3-thiazole-4-carboxylateHCID 67292599—

Reaction Steps

Ethyl 3-bromo-2-oxopropanoate (6.76 mL) was added very carefully to a stirred solution of pentanethioamide (example 78, step e) (6.30 g) in ethanol (100 mL). The solution was then heated at reflux for 16 h. After cooling, the reaction mixture was diluted with ethyl acetate, washed with saturated sodium bicarbonate solution and evaporated in vacuo. Purification by silica gel chromatography eluting with 1:6 ethyl acetate: isohexane gave the subtitled compound as a yellow oil. Yield 6.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-dcb631002a684feea09a269aa421be4e
Source noteuspto-grants-2012_04