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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362257Generated: October 25, 2026

1-(1-Benzofuran-3-yl)ethan-1-one → 1-(Benzofuran-3-yl)-2-bromoethanone

https://huagongshe.com/reaction/362257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Benzofuran-3-yl)ethan-1-oneHCID 11286612—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
SolventTetrahydrofuranHCID 8028—
Product1-(Benzofuran-3-yl)-2-bromoethanoneHCID 277658027.4%

Reaction Steps

A solution of phenyltrimethylammonium tribromide (2.47 g) in tetrahydrofuran (20 ml) was added dropwise at ambient temperature under nitrogen over 5 minutes to a stirred solution of 3-acetylbenzo[b]furan (1 g) in tetrahydrofuran (20 ml), then the mixture was stirred at ambient temperature for a further 1.5 hours, filtered, and the solvent removed in vacuo. The residue was triturated with ether, and the resulting solid was collected by filtration and dried in vacuo at ambient temperature to give 3-(2-bromoacetyl)benzo[b]furan as an off-white solid (0.25 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869492
Source datasetuspto-grants-1999_02
ORD IDord-10b5b665c38b46309fa8f6f6837d9876
Source noteuspto-grants-1999_02