Water → 4-(2,6-Dichloro-4-trifluoromethylphenyl)toluene

HRID 1635737Notes

Reaction equation

HRID 1635737 reaction equation
I[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1.CCCCCC.[Cl:15][C:16]1[CH:17]=[C:18]([C:24]([F:27])([F:26])[F:25])[CH:19]=[C:20]([Cl:23])[C:21]=1F.O>C1C=CC=CC=1.C([Li])CCC.C(OCC)C>[Cl:15][C:16]1[CH:17]=[C:18]([C:24]([F:27])([F:26])[F:25])[CH:19]=[C:20]([Cl:23])[C:21]=1[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1

Participants

8

Reactant 4

HCID 962WaterHCID 8058HexaneHCID 122074-IodotolueneHCID 157026Benzene, 1,3-dichloro-2-fluoro-5-(trifluoromethyl)-

Product 1

HCID 221709614-(2,6-Dichloro-4-trifluoromethylphenyl)tolueneYield 85.1%

Reagents, catalysts & solvents 3

HCID 241BenzeneSolventHCID 3283Diethyl EtherSolventHCID 178418339ButyllithiumSolvent

Procedure

To 5.7 g (26.1 mmol) of 4-iodotoluene in 30 ml of dry benzene, 17.0 ml of a n-butyllithium solution in hexane (1.60 mol/1) was added dropwise in a nitrogen stream at room temperature with stirring. After 2 hours of stirring at room temperature, 10 ml of 6.0 g (25.8 mmol) of 3,5-dichloro-4-fluorobenzotrifluoride in 10 ml of diethyl ether was added dropwise at 10° C. After another 12 hours of stirring at room temperature, the reaction mixture was poured into 100 ml of water for separation. The organic layer was washed with 50 ml of water twice and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 6.7 g of 4-(2,6-dichloro-4-trifluoromethylphenyl)toluene (yield 85.0%) as a colorless liquid.

Workup

  1. stirringAfter 2 hours of stirring at room temperature
  2. stirringAfter another 12 hours of stirring at room temperature
  3. washThe organic layer was washed with 50 ml of water twice
  4. dry with materialdried over anhydrous magnesium sulfate
  5. distillationThe solvent was distilled off under reduced pressure

Sources & evidence

ORD record
ord-08ef1699de1c4ef3a33e8f41c7679ca9
Source dataset
uspto-grants-2003_01
Patent number
US06509354B1

Reaction notes

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