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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403328Generated: November 2, 2026

Hydrochloric Acid → 1-(4-Bromo-2-fluorophenyl)-2-chloroethanone

https://huagongshe.com/reaction/2403328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant4-Bromo-2-fluorobenzoyl chlorideHCID 2734026—
Reactant1-(4-Bromo-3-fluorophenyl)-2-chloroethan-1-oneHCID 53350328—
Reactant4-Bromo-3-fluorophenacyl bromideHCID 53416614—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(4-Bromo-2-fluorophenyl)-2-chloroethanoneHCID 79014947—

Reaction Steps

To a stirred solution of 4-bromo-2-fluorobenzoyl chloride (33 g, CAS 151982-51-3) in acetonitrile (150 ml) and THF (150 ml) at 0-5° C. was added dropwise (trimethylsilyl)diazomethane (83.4 ml, 2 M solution in hexane). The reaction mixture was stirred at room temperature for 30 min. TLC analysis showed the reaction was complete. 37% Hydrochloric acid (23.2 ml) was then added dropwise at 0-5° C. and the reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was then 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 a ca 1:1 mixture of 2-bromo-1-(4-bromo-3-fluoro-phenyl)-ethanone and 2-chloro-1-(4-bromo-3-fluoro-phenyl)-ethanone (34.4 g, 98%) as a yellow solid which was used in the next step without further purification. MS (EI): 203 ([{81Br}M-CH2Cl]+, 201 ([{79Br}M-CH2Cl]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802673B2
Source datasetuspto-grants-2014_08
ORD IDord-ab87fd07f31a4eee9b58ae88dc40cf9f
Source noteuspto-grants-2014_08