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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183589Generated: October 30, 2026

1-(4-Chlorobenzo[b]thien-2-yl)ethanone → HCID 22473621, compound

https://huagongshe.com/reaction/2183589

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Chlorobenzo[b]thien-2-yl)ethanoneHCID 12398628—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22473621HCID 22473621124%

Reaction Steps

A mixture of 1-(4-chlorobenzo[b]thiophen-2-yl]ethan-1-one (1.67 g), phenyltrimethylammonium tribromide (2.98 g) and tetrahydrofuran (40 ml) was stirred under nitrogen at ambient temperature for 22.5 hours then it was filtered and diluted with water (150 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]ethan-1-one (1.65 g) as an off-white solid, m.p. 116-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900216B2
Source datasetuspto-grants-2005_05
ORD IDord-3fcd3f1f0c7443b7baba08706dd00a10
Source noteuspto-grants-2005_05