Reaktion #1339

ord-cfae32b2602f43d987a2a67d53a3bee8

Reaktionsgleichung

CC(C)(C)[O-].[Na+]
Sodium t-butoxide
FC(F)(F)C(Cl)Br
1-bromo-1-chloro-2,2,2-trifluoroethane
CC(C)C=C=O
3-methylbut-1-en-1-al
C1CCOC1
tetrahydrofuran
CC(C)=CC(O)C(Cl)(Br)C(F)(F)F
5-bromo-5-chloro-4-hydroxy-2-methyl-6,6,6-trifluorohex-2-ene

Lösungsmittel

Reaktionsbedingungen

Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturby external cooling under a nitrogen atmosphere
  2. 2
    Temperaturexternal cooling
  3. 3
    Sonstigewas removed
  4. 4
    Sonstigethe reaction quenched by the dropwise addition of saturated aqueous ammonium chloride solution
  5. 5
    SonstigeThe mixture was then partitioned between water and diisopropyl ether
  6. 6
    Sonstigethe aqueous phase separated
  7. 7
    Waschenwashed with diisopropyl ether (3×25 ml)
  8. 8
    WaschenThe organic phase was washed with brine
  9. 9
    Trocknendried over anhydrous sodium sulphate
  10. 10
    Einengenconcentrated by evaporation under reduced pressure
  11. 11
    SonstigeAfter purification by a procedure similar to

Vorschrift

Sodium t-butoxide (1.39 g of a 42% solution in dry dimethyl formamide was added dropwise over a period of 5 minutes to a stirred mixture of 1-bromo-1-chloro-2,2,2-trifluoroethane (0.535 ml), 3-methylbut-1-en-1-al (0.538 ml) and dry tetrahydrofuran (10 ml) maintained at a temperature of -78° C. by external cooling under a nitrogen atmosphere. The mixture was then stirred for a further 40 minutes at the temperature after which the external cooling was removed and the reaction quenched by the dropwise addition of saturated aqueous ammonium chloride solution. The mixture was then partitioned between water and diisopropyl ether and the aqueous phase separated, washed with diisopropyl ether (3×25 ml), and the washings combined with the organic phase. The organic phase was washed with brine and dried over anhydrous sodium sulphate and concentrated by evaporation under reduced pressure. After purification by a procedure similar to that set out in the previous Example there was obtained 5-bromo-5-chloro-4-hydroxy-2-methyl-6,6,6-trifluorohex-2-ene (1.39 g), identified by nuclear magnetic resonance and infra-red spectroscopy.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723649uspto-grants-1998_03