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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436412Generated: November 3, 2026

Hexane → 2-Bromo-1-(4-bromo-2-fluorophenyl)ethanone

https://huagongshe.com/reaction/1436412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantEthyl AcetateHCID 8857—
ReactantBromineHCID 24408—
Reactant1-(4-Bromo-2-fluorophenyl)ethan-1-oneHCID 21938581—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product2-Bromo-1-(4-bromo-2-fluorophenyl)ethanoneHCID 2212148397%

Reaction Steps

Bromine (1.2 mL, 23.0 mmol) in 10 mL of glacial acetic acid was added drop-wise to a solution of 1-(4-bromo-2-fluoro-phenyl)-ethanone (5.0 g, 23.0 mmol), prepared in the previous step, in 150 mL of dry methylene chloride at 0° C. After the addition, the reaction was allowed to warm to room temperature. TLC (5% ethyl acetate:hexane) indicated the starting material was consumed. The reaction was diluted with methylene chloride and washed with 5% sodium thiosulfate and brine. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 2-bromo-1-(4-bromo-2-fluoro-phenyl)-ethanone (6.6 g, 97%) as a light green oil. This compound was used without further purification. MS (ES) m/z 297 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618990B2
Source datasetuspto-grants-2009_11
ORD IDord-f19e8f0b3ac4465a9ce0100b1bdd1b5b
Source noteuspto-grants-2009_11