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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25283Generated: October 27, 2026

Water → [3-(2,6-Dichloro-4-trifluoromethylphenyl)phenyl]isopropyl sulfide

https://huagongshe.com/reaction/25283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzene, 1,3-dichloro-2-fluoro-5-(trifluoromethyl)-HCID 157026—
Reactant1-Iodo-3-[(1-methylethyl)thio]benzeneHCID 22170941—
ReactantButyllithiumHCID 178418339—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product[3-(2,6-Dichloro-4-trifluoromethylphenyl)phenyl]isopropyl sulfideHCID 2217093638%

Reaction Steps

1.0 g (3.6 mmol) of 3-iodophenyl isopropyl sulfide was stirred in 10 ml of dry benzene in a nitrogen stream at room temperature, while 2.8 ml of a n-butyllithium solution in hexane (1.56 mol/l) was added dropwise. The resulting reaction mixture was stirred at room temperature for another 2 hours and cooled to 10° C., and 1.0 g (4.3 mmol) of 3,5-dichloro-4-fluorobenzotrifluoride in 50 ml of diethyl ether was added dropwise. The resulting reaction mixture was stirred at room temperature for further 12 hours and poured into 100 ml of water for separation. The organic layer was washed with 50 ml of water twice and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 0.5 g of [3-(2,6-dichloro-4-trifluoromethylphenyl)phenyl] isopropyl sulfide (yield 38.0%) as a colorless liquid (nD20 1.5675).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858639B2
Source datasetuspto-grants-2005_02
ORD IDord-cf39dcdcfd37478aa9cd71b7049c8432
Source noteuspto-grants-2005_02