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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25306Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/25306

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1-Chloro-3-iodobenzeneHCID 12269—
EduktBenzene, 1,3-dichloro-2-fluoro-5-(trifluoromethyl)-HCID 157026—
LösungsmittelBenzeneHCID 241—
LösungsmittelHexaneHCID 8058—
LösungsmittelButyllithiumHCID 178418339—
Produkt1-Chloro-3-(2,6-dichloro-4-trifluoromethylphenyl)benzeneHCID 2217092636,7%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858639B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-f2cfb412bf3d4b57a1c11a5247038448
Quellennotizuspto-grants-2005_02