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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Chloro-3-iodobenzene | HCID 12269 | — |
| Reactant | Benzene, 1,3-dichloro-2-fluoro-5-(trifluoromethyl)- | HCID 157026 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Butyllithium | HCID 178418339 | — |
| Product | 1-Chloro-3-(2,6-dichloro-4-trifluoromethylphenyl)benzene | HCID 22170926 | 36.7% |
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
| 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-f2cfb412bf3d4b57a1c11a5247038448 |
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| Source note | uspto-grants-2005_02 |
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