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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25279Generated: October 25, 2026

Water → [5-(2,6-Dichloro-4-trifluoromethylphenyl)-2-methylphenyl]isopropyl sulfide

https://huagongshe.com/reaction/25279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsopropyl iodideHCID 6362—
Reactant1,1'-Thiodi-[5-(2,6-dichloro-4-trifluoromethylphenyl)-2-methylbenzene]HCID 22170944—
ReactantSodium Formaldehyde SulfoxylateHCID 23689980—
SolventDimethylformamideHCID 6228—
Product[5-(2,6-Dichloro-4-trifluoromethylphenyl)-2-methylphenyl]isopropyl sulfideHCID 1213764275.3%

Reaction Steps

3.3 g (4.9 mmol) of 1,1′-thiodi-[5-(2,6-dichloro-4-trifluoromethylphenyl)-2-methylbenzene], 3.0 g (19.5 mmol) of Rongalite and 3.0 g (17.6 mmol) of isopropyl iodide were stirred in 30 ml of N,N-dimethylformamide at room temperature for 3 hours. The resulting reaction mixture was poured into 300 ml of water and extracted with 50 ml of ethyl acetate twice. The ethyl acetate layer was washed with 50 ml of water twice and dtied over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 1.4 g of [5-(2,6-dichloro-4-trifluoromethylphenyl)-2-methylphenyl] isopropyl sulfide (yield 38.0%) as a yellow dough (nD20 1.5462).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858639B2
Source datasetuspto-grants-2005_02
ORD IDord-6874889d9b6847a0840fc9cf974c3a49
Source noteuspto-grants-2005_02