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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183644Generated: October 30, 2026

Phenyltrimethylammonium bromide dibromide → 2-Bromo-1-(4-chlorobenzo[b]thiophen-2-yl)butan-1-one

https://huagongshe.com/reaction/2183644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
Reactant1-(4-Chlorobenzo[b]thiophen-2-yl)butan-1-oneHCID 22473690—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-1-(4-chlorobenzo[b]thiophen-2-yl)butan-1-oneHCID 22473997148.6%

Reaction Steps

A mixture of 1-(4-chlorobenzo[b]thiophen-2-yl)butan-1-one (0.93 g), phenyltrimethylammonium tribromide (1.47 g) and tetrahydrofuran (20 ml) was stirred under nitrogen at ambient temperature for 66 hours, then it was filtered and diluted with water (50 ml). The product was extracted into dichloromethane (3×30 ml), the combined extracts were dried (MgSO4) and the solvents were removed in vacuo. The residue was purified by flash chromatography over silica using dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to leave 2-bromo-1-(4-chlorobenzo[b]thiophen-2-yl)butan-1-one (1.07 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900216B2
Source datasetuspto-grants-2005_05
ORD IDord-a456adcc477d42818d7603c3c6875f78
Source noteuspto-grants-2005_05