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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Benzene, 1,3-dichloro-2-fluoro-5-(trifluoromethyl)- | HCID 157026 | — |
| Reactant | 1-Iodo-3-[(1-methylethyl)thio]benzene | HCID 22170941 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | [3-(2,6-Dichloro-4-trifluoromethylphenyl)phenyl]isopropyl sulfide | HCID 22170936 | 38% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858639B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-cf39dcdcfd37478aa9cd71b7049c8432 |
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| Source note | uspto-grants-2005_02 |
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