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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635742Generated: October 26, 2026

Water → 1-Chloro-3-(2,6-dichloro-4-trifluoromethylphenyl)benzene

https://huagongshe.com/reaction/1635742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexaneHCID 8058—
Reactant1-Chloro-3-iodobenzeneHCID 12269—
ReactantBenzene, 1,3-dichloro-2-fluoro-5-(trifluoromethyl)-HCID 157026—
SolventBenzeneHCID 241—
SolventButyllithiumHCID 178418339—
Product1-Chloro-3-(2,6-dichloro-4-trifluoromethylphenyl)benzeneHCID 2217092636.7%

Reaction Steps

To 10.0 g (41.9 mmol) of 1-chloro-3-iodobenzene in 50 ml of dry benzene, 32.0 ml of a n-butyllithium solution in hexane (1.56 mol/1) was added dropwise in a nitrogen stream at room temperature with stirring. After another 2 hours of stirring at room temperature, 9.9 g (42.5 mmol) of 3,5-dichloro-4-fluorobenzotrifluoride was added dropwise at 10° C. After another 12 hours of stirring at room temperature, the reaction mixture was poured into 500 ml of water for separation. The organic layer was washed with 200 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 5.0 g of 1-chloro-3-(2,6-dichloro-4-trifluoromethylphenyl)benzene (yield 35.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509354B1
Source datasetuspto-grants-2003_01
ORD IDord-a0faa94efe7d4b90a61c33432f202973
Source noteuspto-grants-2003_01