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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618974Generated: October 31, 2026

1-(4-Bromo-2-thienyl)ethan-1-one → 2-Bromo-1-(4-bromo-2-thienyl)ethanone

https://huagongshe.com/reaction/1618974

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromo-2-thienyl)ethan-1-oneHCID 2735237—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-Bromo-1-(4-bromo-2-thienyl)ethanoneHCID 12890346—

Reaction Steps

To 1-(4-bromothiophen-2-yl)ethanone (10 g, 48.8 mmol) in methanol (98 mL) and dichloromethane (163 mL) is added tetra-n-butylammonium tribromide (28.8 g, 58.5 mmol). The reaction mixture is concentrated under reduced pressure at 50° C. to give a residue which is purified by silica gel chromatography, eluting with dichloromethane to give crude 2-bromo-1-(4-bromo-2-thienyl)ethanone. To a solution of the crude 2-bromo-1-(4-bromo-2-thienyl)ethanone in acetonitrile (200 ml) is added potassium carbonate (20.2 g, 146 mmol) and diallylamine (9.48 g, 97.5 mmol). The reaction is stirred at room temperature for 2 hours. Water is added and the solution is extracted with ethyl acetate. The organic phases are combined, dried over sodium sulfate, filtered, and concentrated under reduced pressure to give the crude title compound. ES/MS (m/e): (79Br/81Br) 300/302 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772282B2
Source datasetuspto-grants-2014_07
ORD IDord-7e76881104b8435cbc3a87382a58953e
Source noteuspto-grants-2014_07