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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114388Generated: October 31, 2026

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

https://huagongshe.com/reaction/2114388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1-(4-Bromo-2-fluorophenyl)ethan-1-oneHCID 21938581—
SolventChloroformHCID 6212—
Product2-Bromo-1-(4-bromo-2-fluorophenyl)ethanoneHCID 2212148389.2%

Reaction Conditions

Temperature5 °C

Reaction Steps

1-(4-Bromo-2-fluorophenyl)ethanone (2.59 g, 11.9 mmol, 1.00 equiv) was dissolved in chloroform (5 mL) and cooled to 5° C. Bromine (0.613 mL, 11.9 mmol, 1.00 equiv) was added dropwise via syringe. On completion of the addition, the bath was removed and the reaction was allowed to warm to room temperature. After two hours, the reaction was poured onto ice and diluted with EtOAc. The mixture was washed sequentially with saturated NaHCO3, water, and saturated NaCl. The organic phase was dried over Na2SO4, filtered and concentrated to afford 3.14 g (89%) of a white solid. 1H NMR (CDCl3) 7.92-7.83 (m, 1H), 7.51-40 (m, 2H), 4.50 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432258B2
Source datasetuspto-grants-2008_10
ORD IDord-1c2fa2f7af05438492838499a2671fae
Source noteuspto-grants-2008_10