4-tert-Butylcyclohexanone → 4-tert-butyl-1,1-difluorocyclohexane

HRID 1193002Notes

Reaction equation

HRID 1193002 reaction equation
F[B-](F)(F)F.[FH:6].[FH:7].F.C(N(CC)CC)C.C(N(CC)CC)C.[C:23]([CH:27]1[CH2:32][CH2:31][C:30](=O)[CH2:29][CH2:28]1)([CH3:26])([CH3:25])[CH3:24].C(=O)(O)[O-].[Na+]>ClCCl>[C:23]([CH:27]1[CH2:32][CH2:31][C:30]([F:7])([F:6])[CH2:29][CH2:28]1)([CH3:26])([CH3:25])[CH3:24]

Participants

7

Procedure

To a mixture of diethylaminosulfinium tetrafluoroborate (344 mg, 1.5 mmol), triethylamine trihydrofluoride (326 μl, 2.0 mmol) and triethylamine (139 μl, 1.0 mmol) in dichloromethane (3.0 mL) at room temperature is added 4-tert-butylcyclohexanone (154 mg, 1.0 mmol). The reaction mixture is stirred for 22 hours, then an aqueous solution of sodium bicarbonate (5%) is added and stirring is continued for 15 minutes. The phases are separated and the aqueous layer is extracted twice using dichloromethane. The organic phases are combined and dried with magnesium sulphate. The solution is passed through a pad of silica gel with dichloromethane elution. Solvent are evaporated in vacuo to provide 4-t-butyl-1,1-difluorocyclohexane (160 mg, 91%) as a clear liquid, admixed with 0.8% of the corresponding vinyl fluoride.

Workup

  1. stirringstirring
  2. waitis continued for 15 minutes
  3. customThe phases are separated
  4. extractionthe aqueous layer is extracted twice using dichloromethane
  5. dry with materialdried with magnesium sulphate
  6. washThe solution is passed through a pad of silica gel with dichloromethane elution
  7. customSolvent are evaporated in vacuo

Sources & evidence

ORD record
ord-7c3bfa32783c4db38afde6c3e6691cb7
Source dataset
uspto-grants-2014_03
Patent number
US08680332B2

Reaction notes

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