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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571815Generated: October 29, 2026

Hydrochloric Acid → 1261859-54-4

https://huagongshe.com/reaction/571815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant4-Bromo-3-chlorobenzoyl chlorideHCID 19754905—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
Product1261859-54-4HCID 5335032795%

Reaction Steps

To a stirred solution of 4-bromo-3-chlorobenzoyl chloride (11 g, CAS 21900-32-3) in acetonitrile (50 ml) and THF (50 ml) at 0-5° C. was added dropwise (trimethylsilyl)diazomethane (26.0 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 (7.22 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 1-(4-bromo-3-chlorophenyl)-2-chloroethanone (11.0 g, 95%) as a light brown solid which was used in the next step without further purification. MS (EI): 221 ([{81Br37Cl}M-CH2Cl]+), 219 ([{79Br37Cl/81Br35Cl}M-CH2Cl]+), 217 ([{79Br35Cl}M-CH2Cl]+), 193 ([{81Br37Cl}M-CH2Cl—CO]+), 191 ([{79Br37Cl/81Br35Cl}M-CH2Cl—CO]+), 189 ([{79Br35Cl}M-CH2Cl—CO]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029370B2
Source datasetuspto-grants-2015_05
ORD IDord-aaa0c5604b58443dafb5677fe4532923
Source noteuspto-grants-2015_05