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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405382Generated: November 2, 2026

5-Bromo-7-fluoro-1-benzofuran-2-carboxylic acid → 5-Bromo-7-fluorobenzofuran

https://huagongshe.com/reaction/2405382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-7-fluoro-1-benzofuran-2-carboxylic acidHCID 62379218—
CatalystCopperHCID 23978—
SolventQuinolineHCID 7047—
Product5-Bromo-7-fluorobenzofuranHCID 22144820102.2%

Reaction Steps

A solution of 5-bromo-7-fluoro-1-benzofuran-2-carboxylic acid (1.274 mmol) in quinoline (2 mL) was treated with copper dust (0.236 mmol). The reaction was purged with nitrogen, sealed and irradiated in a microwave reactor at 230° C. for 60 min. The solution was diluted with ethyl acetate and was filtered through Celite. The filtrate was concentrated in vacuo, and the residue was purified by flash chromatography (hexanes) to provide the title compound as a clear oil (280 mg, 100% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 8.17 (d, J=2.02 Hz, 1H) 7.77 (d, J=1.77 Hz, 1H) 7.55 (dd, J=10.48, 1.64 Hz, 1H) 7.07 (dd, J=3.16, 2.15 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802864B2
Source datasetuspto-grants-2014_08
ORD IDord-10f1d137e3c64bb3baf7368d1f2ee6cd
Source noteuspto-grants-2014_08