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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Chlorothiophenol | HCID 7815 | — |
| Reactant | 2-Bromo-4-trifluoromethylaniline | HCID 93899 | — |
| Reactant | 2-Bromo-1-iodo-4-(trifluoromethyl)benzene | HCID 16244089 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Bis[2-(diphenylphosphino)phenyl] ether | HCID 4285986 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Bromo-2-(4-chlorophenylsulfanyl)-5-(trifluoromethyl)benzene | HCID 68683413 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732463B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-d9347c96bc4843159a6b8f6dab67a98c |
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| Source note | uspto-grants-2010_06 |
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