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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322028Generated: October 30, 2026

2-(2-Bromophenoxy)-1-phenylethan-1-one → 7-Bromo-3-phenylbenzofuran

https://huagongshe.com/reaction/322028

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Bromophenoxy)-1-phenylethan-1-oneHCID 3016354—
SolventWaterHCID 962—
Product7-Bromo-3-phenylbenzofuranHCID 301635578.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 2-(2-bromophenoxy)-1-phenyl-1-ethanone (6.31 g) and polyphosphoric acid (285 g) was stirred at 95° C. for 6 h. The resulting solution was cooled to 50° C. , poured in water (2 L), extracted with Et2O (2×1 L). The combined organic extracts were washed with water (4×500 ml) and brine, dried over MgSO4 and concentrated. The residual solid was filtered on a plug of silica gel using Et2O. Recrystallization in hot hexane yielded the title compound (4.63g; 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211197B1
Source datasetuspto-grants-2001_04
ORD IDord-6cdbed8943fb48f68118e840327e7135
Source noteuspto-grants-2001_04