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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25306Generated: October 25, 2026

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

https://huagongshe.com/reaction/25306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Chloro-3-iodobenzeneHCID 12269—
ReactantBenzene, 1,3-dichloro-2-fluoro-5-(trifluoromethyl)-HCID 157026—
SolventBenzeneHCID 241—
SolventHexaneHCID 8058—
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/l) 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 numberUS06858639B2
Source datasetuspto-grants-2005_02
ORD IDord-f2cfb412bf3d4b57a1c11a5247038448
Source noteuspto-grants-2005_02