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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254807Generated: October 30, 2026

Bromine → Ethyl 4-bromo-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/254807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantEthyl 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1h-pyrazole-3-carboxylateHCID 10905332—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-bromo-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1H-pyrazole-3-carboxylateHCID 1093968445.7%

Reaction Steps

To a solution of ethyl 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1H-pyrazole-3-carboxylate (1 g, 2.4 mmol) in methylene chloride (30 ml) at room temperature was added bromine (4.9 ml, prepared 1.0 M solution in methylenechlordie, 4.9 mmol) dropwisely. The reaction mixture was stirred at room temperature for 1 hour and the resulting solution was diluted with ethyl ether (50 ml). The reaction mixture was quenched with saturated sodium bicarbonate solution (30 ml) and extracted with ethyl ether (50 ml twice). The organic solution was evaporated under reduced pressure, and crude residue was purified with silica gel column (hexane/ethyl acetate=5/1) to recover starting material (401 mg, 40%) and produce the title compound (520 mg, 45% yield) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875647B2
Source datasetuspto-grants-2011_01
ORD IDord-b959295677fe429ca6fa848aa4a0b427
Source noteuspto-grants-2011_01