Reaktion #2254203

ord-6e04ebacc15b4e438e419dc49931b4f5

Reaktionsgleichung

O
H2O
[K+].[OH-]
KOH
COC(=O)C(C#N)C1(c2ccc(F)cc2)CCOCC1
methyl 2-cyano-2-[4-(4-fluorophenyl)oxan-4-yl]acetate
N#CCC1(c2ccc(F)cc2)CCOCC1
2-[4-(4-fluorophenyl)oxan-4-yl]acetonitrile

Lösungsmittel

Reaktionsbedingungen

Temperatur
120°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled
  2. 2
    Extraktionthe product extracted with Et2O (3×50 ml)
  3. 3
    Waschenwashed with H2O (50 ml)
  4. 4
    Sonstigedried over NA2SO4
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated
  7. 7
    SonstigePurified by normal phase SiO2 chromatography (5 to 40% EtOAc/hexanes)

Vorschrift

To a pre-dissolved solution of KOH (441 mg, 7.87 mmol) in ethylene glycol (20 ml) was added methyl 2-cyano-2-[4-(4-fluorophenyl)oxan-4-yl]acetate (1.09 g, 3.93 mmol). The mixture was heated to 120° C. for 3 h, and then cooled. H2O was added (50 ml), the product extracted with Et2O (3×50 ml), washed with H2O (50 ml), dried over NA2SO4, filtered and concentrated. Purified by normal phase SiO2 chromatography (5 to 40% EtOAc/hexanes) to give 2-[4-(4-fluorophenyl)oxan-4-yl]acetonitrile as a colorless oil (450 mg, 78%, m/z: 219.1 [M+H]+ observed).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09044469B2uspto-grants-2015_06