12,12-Difluoro-11-dodecen-2-ol → Methyl 10,10-difluoro-9-decenyl ketone

HRID 1090450Notes

Reaction equation

HRID 1090450 reaction equation
[F:1][C:2]([F:15])=[CH:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH:12]([OH:14])[CH3:13].CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O>CC(C)=O>[F:1][C:2]([F:15])=[CH:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]([CH3:13])=[O:14]

Participants

4

Procedure

To a stirred solution of 1.0 gram (0.0045 mole) of 12,12-difluoro-11-dodecen-2-ol (prepared in Example 3) in 10 ml of acetone was added 1.68 ml (0.0045 mole) of Jones reagent (2.7 Molar in acetone) while maintaining the reaction mixture temperature at 20°-25° C. Excess Jones reagent was destroyed by the addition of 1-methylethanol. The reaction mixture was passed through silica gel with the aid of additional acetone. The eluate was concentrated under reduced pressure, and the residue was dissolved in 50 ml of pentane. The resultant solution was washed with two 20 ml portions of water and then with one 20 ml portion of an aqueous solution saturated with sodium chloride. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure yielding 0.65 gram of methyl 10,10-difluoro-9-decenyl ketone. The nmr spectrum was consistent with the proposed structure. The reaction was repeated several times.

Workup

  1. temperaturewhile maintaining the reaction mixture temperature at 20°-25° C
  2. customExcess Jones reagent was destroyed by the addition of 1-methylethanol
  3. concentrationThe eluate was concentrated under reduced pressure
  4. dissolutionthe residue was dissolved in 50 ml of pentane
  5. washThe resultant solution was washed with two 20 ml portions of water
  6. dry with materialThe organic layer was dried with magnesium sulfate
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-88aeec64fe9b438ebfcfdda8272ff1d2
Source dataset
uspto-grants-1992_01
Patent number
US05081287

Reaction notes

Loading…