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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424390Generated: October 25, 2026

2-Acetylthiophene → Ethyl 3-oxo-3-(thiophen-2-yl)propanoate

https://huagongshe.com/reaction/424390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AcetylthiopheneHCID 6920—
ReactantDiethyl CarbonateHCID 7766—
ReactantSodium hydrideHCID 24758—
ProductEthyl 3-oxo-3-(thiophen-2-yl)propanoateHCID 255159—

Reaction Conditions

Temperature71 °C

Reaction Steps

To a solution of 1-(thiophen-2-yl)ethanone (2.944 g, 23.3 mmol) and Diethyl carbonate (70 mL) at 0° C. was added sodium hydride (1.86 g, 46.6 mmol). The resulting off-white slurry solution was gradually warmed to 71° C., and stirred for 1.5 hour. The reaction mixture was poured into ice-HOAc—H2O, and extracted with ethyl acetate. The organic phase was washed (brine), dried (MgSO4) and concentrated to give a brown liquid. The crude product was purified via flash chromatography (silica gel cartridge with eluent of 0-3% ethyl acetate/hexane) to afford ethyl 3-oxo-3-(thiophen-2-yl)propanoate as an amble liquid, 4.193 g (91%). LCMS m/z 388.99, 390.09 (M+23); HPLC: Rt 2.01 min. (4.0 min. gradient, Column: YMC Combiscreen C-18, Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106046B2
Source datasetuspto-grants-2012_01
ORD IDord-4227d811ef7a42908acad62aba526e0a
Source noteuspto-grants-2012_01