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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108303Generated: November 1, 2026

Water → (4-Bromo-7-methoxybenzofuran-2-yl)-cyclopropyl-methanone

https://huagongshe.com/reaction/1108303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
ReactantCyclopropyl-(7-methoxybenzofuran-2-yl)-methanoneHCID 18784859—
SolventAcetonitrileHCID 6342—
Product(4-Bromo-7-methoxybenzofuran-2-yl)-cyclopropyl-methanoneHCID 1878485570.3%

Reaction Steps

N-bromosuccinimide (0.21 g) was added in a single portion to a stirred solution of cyclopropyl-(7-methoxybenzofuran-2-yl)-methanone (0.25 g) in acetonitrile (20 ml) under an atmosphere of nitrogen. The reaction mixture was stirred at room temperature for 24 h. Water (20 ml) was added, the mixture extracted with ethyl acetate (100 ml), the organic layer separated, dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by flash chromatography on silica eluting with 5-10% ethyl acetate in hexane afforded the title compound as an off-white solid (0.24 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066657
Source datasetuspto-grants-2000_05
ORD IDord-5bf4a7643b024c5b913e075851dc6d83
Source noteuspto-grants-2000_05