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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402919Generated: November 1, 2026

Water → 2-benzoyl-5-chlorobenzofuran

https://huagongshe.com/reaction/1402919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenacyl bromideHCID 6259—
Reactant5-Chloro-salicylaldehydeHCID 12481—
SolventEthanolHCID 702—
Product2-benzoyl-5-chlorobenzofuranHCID 402026377.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 5-chloro-2-hydroxybenzaldehyde (2 g) and phenacyl bromide (1.85 g) in ethanol (10 ml) potassium carbonate (3.53 g) was added. The mixture was stirred at 80° C. for 1 h. Then the reaction mixture was poured into water (50 ml) and extracted with dichloromethane (3×20 ml). The combined organic layers were washed with brine (20 ml), dried (MgSO4), and concentrated under reduced pressure. The crude was purified by flash chromatography on silica gel (hexane/ethyl acetate 12:1) to give 2-benzoyl-5-chlorobenzofuran (1.85 g) as colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912186B2
Source datasetuspto-grants-2014_12
ORD IDord-fff25e4fc43a44a3a51b021cae092819
Source noteuspto-grants-2014_12