HCID 20354850, Verbindung → HCID 20354859, Verbindung

HRID 1580781Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1580781
[C:1]([O:4][CH:5]([CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])[CH2:6][CH2:7][C:8]12O[CH:12]1[CH2:11][CH2:10][C:9]2=[O:14])(=[O:3])[CH3:2]>C(O)(=O)C>[C:1]([O:4][CH:10]1[C:9](=[O:14])[C:8]([CH2:7][CH2:6][CH:5]([O:4][C:1](=[O:3])[CH3:2])[CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])=[CH:12][CH2:11]1)(=[O:3])[CH3:2]

Komponenten

3

Versuchsvorschrift

A solution of 2-(3-acetoxyoctyl)-2,3-epoxycyclopentanone (26.8 g.)[prepared as described in (g) above] in glacial acetic acid (500 ml.) was heated at reflux for 12 hours. The excess acetic acid was then removed in vacuo and the residue distilled under reduced pressure to give 5-acetoxy-2-(3-acetoxyoctyl)cyclopent-2-enone (24.7 g.), b.p. 164°-175°C./0.2 mm.Hg.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureat reflux for 12 hours
  3. customThe excess acetic acid was then removed in vacuo
  4. distillationthe residue distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-9210e3e9b9a742308a35bf8d1c2dedd9
Quelldatensatz
uspto-grants-1976_01
Patentnummer
US03933890

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