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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443368Generated: October 25, 2026

1-(2-Bromo-4-fluorophenyl)ethan-1-one → 2-Bromo-1-(2-bromo-4-fluorophenyl)ethanone

https://huagongshe.com/reaction/1443368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Bromo-4-fluorophenyl)ethan-1-oneHCID 2736304—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-1-(2-bromo-4-fluorophenyl)ethanoneHCID 2186494863%

Reaction Steps

To 1-(2-Bromo-4-fluoro-phenyl)-ethanone (2.5 g, 11.52 mmol) in anhydrous tetrahydrofuran (53 mL) under argon was added phenyltrimethylammonium tribromide (4.33 g, 11.52 mmol, 1.0 eq) at 0° C. The reaction mixture was stirred at ambient temperature for 16 h, concentrated, and re-dissolved in ethyl acetate. The organic layer was washed with water (2×150 mL) and brine (1×100 mL), dried (MgSO4), filtered, and evaporated in vacuo. Purification using MPLC chromatography (Biotage) gave 2.14 g (63%) of 2-bromo-1-(2-bromo-4-fluoro-phenyl)-ethanone as a clear oil. 1H-NMR (CD2Cl2) δ 7.57 (dd, J=9.6 Hz, 1H), 7.44 (dd, J=8, 2 Hz, 1H), 7.21 (m, 7.21-7.14, 1H), 4.51 (s, 2H); TLC Rf=0.38, 15% ethyl acetate-hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659412B2
Source datasetuspto-grants-2010_02
ORD IDord-0edda7eab2064da5a9438c70c867480c
Source noteuspto-grants-2010_02