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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401135Generated: October 25, 2026

Bromobenzene → 1-Phenyl-2-(thiophen-3-yl)ethanone

https://huagongshe.com/reaction/401135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-methoxy-N-methyl-2-(thiophen-3-yl)acetamideHCID 11423995—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-Phenyl-2-(thiophen-3-yl)ethanoneHCID 1223311355%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To the solution of bromo-benzene (1.0 g, 6.36 mmol) in anhydrous THF (30 mL) was added n-BuLi (5.9 mmol, 2.4 mL) at −78° C. under nitrogen, and the mixture was stirred at −78° C. for further 20 min., a solution of N-methoxy-N-methyl-2-(thiophen-3-yl)acetamide (1 g, 5.4 mmol) in anhydrous THF (10 mL) was added. The resulting mixture was stirred at −78° C. under nitrogen for about 30 min., poured into NH4Cl aqueous solution, and extracted with EtOAc. The organic layers were washed with brine, dried over sodium sulfate, concentrated, and purified by column chromatograph (PE:EtOAc=20:1) to afford Intermediate 2 as a colorless oil (600 mg, yield 55.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741915B2
Source datasetuspto-grants-2014_06
ORD IDord-a89dfd87cb0842c393f81dc108631a7c
Source noteuspto-grants-2014_06