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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269707Generated: October 30, 2026

Ethanol → Ethyl 3-[4-(2-benzofuranyl)thiazol-2-yl]propionate

https://huagongshe.com/reaction/2269707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1-(1-Benzofuran-2-Yl)-2-Bromoethan-1-OneHCID 2735451—
ReactantMethyl 4-amino-4-thioxobutanoateHCID 18333020—
SolventWaterHCID 962—
ProductEthyl 3-[4-(2-benzofuranyl)thiazol-2-yl]propionateHCID 18333015—

Reaction Steps

2-(Bromoacetyl)benzofuran (650 ml) was added to an ethanol (12 ml) solution of methyl 4-amino-4-thioxobutyrate (400 mg), which was heated under reflux overnight. After cooling, water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was dried, concentrated, and then purified by silica gel column chromatography (eluent: hexane/ethyl acetate=4/1). The obtained crystals were washed with hexane to obtain ethyl 3-[4-(2-benzofuranyl)thiazol-2-yl]propionate (460 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329389B1
Source datasetuspto-grants-2001_12
ORD IDord-81ba8f4e2d634cbfbf9dcde51199b65d
Source noteuspto-grants-2001_12