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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15192Generated: October 23, 2026

p-Chlorothiophenol → 1-Bromo-2-(4-chlorophenylsulfanyl)-5-(trifluoromethyl)benzene

https://huagongshe.com/en/reaction/15192

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ChlorothiophenolHCID 7815—
Reactant2-Bromo-4-trifluoromethylanilineHCID 93899—
Reactant2-Bromo-1-iodo-4-(trifluoromethyl)benzeneHCID 16244089—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
SolventTolueneHCID 1140—
Product1-Bromo-2-(4-chlorophenylsulfanyl)-5-(trifluoromethyl)benzeneHCID 6868341381%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of tris(dibenzylidene)dipalladium(0) (Pd2dba3, 0.183 g, 0.2 mmol) and bis(2-diphenylphosphinophenyl)ether (DPEphos, 0.215 g, 0.2 mmol) in toluene (80 mL) was added 3-bromo-4-iodobenzotrifluoride (7.02 g, 20 mmol; prepared from 2-bromo-4-trifluoromethyl-phenylamine by diazotization according to the general procedure by Tunney and Stille J. Org. Chem. 1987, 52, 748-753), 4-chlorothiophenol (2.89 g, 20 mmol) and potassium tert-butoxide (2.46 g, 22 mmol) at room temperature (rt). The reaction mixture was stirred for 2.5 h at 100° C. and then cooled to room temperature (rt) and filtered through celite. The solvent was evaporated off and the crude product was purified by flash chromatography on silica gel (eluent: ethyl acetate/heptane 2:8) to produce 4.53 g (81%) of 1-bromo-2-(4-chloro-phenylsulfanyl)-5-(trifluoromethyl)-benzene as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732463B2
Source datasetuspto-grants-2010_06
ORD IDord-d9347c96bc4843159a6b8f6dab67a98c
Source noteuspto-grants-2010_06