Reaktion #6564

ord-7f55e0a2549a42539e09fd9289ec2f3a

Reaktionsgleichung

CN(C)P(N(C)C)N(C)C
Tris(dimethylamino)phosphine
FC(F)(Br)Br
dibromodifluoromethane
CC(=O)CCCC(=O)OCc1ccccc1
benzyl 5-oxohexanoate
CC(CCCC(=O)OCc1ccccc1)=C(F)F
Benzyl 6,6-difluoro-5-methyl-5-hexenoate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturmaintained under a nitrogen atmosphere
  2. 2
    Temperaturice bath cooling
  3. 3
    workup.ADDITIONwas added slowly
  4. 4
    SonstigeThe ice bath was then removed
  5. 5
    workup.WAITto stand overnight
  6. 6
    workup.ADDITIONpoured into 200 ml ice water
  7. 7
    Extraktionextracted with ether
  8. 8
    WaschenThe ether phase was washed twice with water
  9. 9
    Trocknendried over sodium sulphate
  10. 10
    Filtrationfiltered
  11. 11
    Einengenconcentrated in a rotary evaporator
  12. 12
    workup.DISTILLATIONThe residue was distilled under reduced pressure

Vorschrift

27.85 g Tris(dimethylamino)phosphine was added dropwise to a solution of 17.90 g dibromodifluoromethane in 130 ml diglyme, maintained under a nitrogen atmosphere and ice bath cooling. After stirring for one hour on the ice bath, 8.82 g benzyl 5-oxohexanoate in 70 ml diglyme was added slowly, dropwise. The ice bath was then removed and the reaction mixture stirred for 3 hours at room temperature, allowed to stand overnight, poured into 200 ml ice water and extracted with ether. The ether phase was washed twice with water, dried over sodium sulphate, filtered and concentrated in a rotary evaporator. The residue was distilled under reduced pressure.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05248810uspto-grants-1993_09