Reaktion #4083

ord-8fa7272f95be4725909831043f7554af

Reaktionsgleichung

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C=CC4=CC(=O)C=C[C@]4(C)[C@H]3CC[C@]12C
cholesta-1,4,6-trien-3-one
[K]
potassium
C=C(C)OC(C)=O
isopropenyl acetate
→
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=CC=C4CC(O)C=C[C@]4(C)[C@H]3CC[C@]12C
cholesta-1,5,7-trien-3-ol
Ausbeute 58.0%

Edukte

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C=CC4=CC(=O)C=C[C@]4(C)[C@H]3CC[C@]12C
cholesta-1,4,6-trien-3-one
[K]
potassium
C=C(C)OC(C)=O
isopropenyl acetate

Reagenzien

Keine

Lösungsmittel

CCCCOC(C)=O
butyl acetate

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe resulting mixture was heated
  2. 2
    Temperaturunder reflux for 7 hours
  3. 3
    SonstigeAfter completion of the reaction

Vorschrift

To a mixture of 19 g (0.05 mol) of cholesta-1,4,6-trien-3-one (I), 6.8 g (0.05 mol) of potassium acid sulphate and 200 g (2 mol) of isopropenyl acetate were added 200 ml of butyl acetate, and the resulting mixture was heated under reflux for 7 hours. After completion of the reaction, the same treatment as in Example 1 was carried out to yield 11.1 g of cholesta-1,5,7-trien-3-ol (IV). The yield was 58%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04723045uspto-grants-1988_02