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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571805Generated: October 31, 2026

Hydrochloric Acid → 1-(4-Bromo-3-fluorophenyl)-2-chloroethan-1-one

https://huagongshe.com/reaction/571805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant4-Bromo-3-fluorobenzoyl chlorideHCID 22626891—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Bromo-3-fluorophenyl)-2-chloroethan-1-oneHCID 53350328—

Reaction Steps

To a stirred solution of 4-bromo-3-fluorobenzoyl chloride (5.6 g, CAS 695188-21-7) in acetonitrile (30 ml) and THF (30 ml) at 0-5° C. was added dropwise (trimethylsilyl)diazomethane (13.7 ml, 2 M solution in diethyl ether). The reaction mixture was stirred at room temperature for 30 min TLC analysis showed the reaction was complete. Hydrochloric acid (3.81 ml, 37% aq.) was then added dropwise at 0-5° C. over 10 minutes and the reaction mixture was then stirred at room temperature for a further 20 minutes. The reaction mixture was poured into EtOAc and extracted sequentially with aq. Na2CO3 solution, water and saturated brine. The organic layer was then dried over Na2SO4 and concentrated in vacuo to afford 2-chloro-1-(4-bromo-3-fluoro-phenyl)-ethanone (5.67 g) as a yellow solid which was used in the next step without further purification. MS (EI): 203 ([{81Br}M-CH2Cl]+), 201 ([{79Br}M-CH2Cl]+), 175 ([{81Br}M-CH2Cl—CO]+), 173 ([{79Br}M-CH2Cl—CO]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029370B2
Source datasetuspto-grants-2015_05
ORD IDord-720a69f1cfd34442af2331b80ca307e8
Source noteuspto-grants-2015_05