Reaktionsgleichung
OC1CCCCCCCCC=CCCCCCCCCC1=O.[OH:23][CH:24]1[CH2:47][CH2:46][CH2:45][CH2:44][CH2:43][CH2:42][CH2:41][CH2:40][CH2:39][CH2:38][CH:37]=[CH:36][CH2:35][CH2:34][CH2:33][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][C:25]1=[O:48]>>[OH:48][CH:25]1[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][C:24]1=[O:23]Komponenten
3
Versuchsvorschrift
2-Hydroxy-11-cycloeicosenone of Synthesis Example 7 was replaced by 2-hydroxy-13-cyclotetracosenone (0.70 g, 1.92 mmol). The latter was subjected to a hydrogenation reaction and subsequent treatment under the same conditions as in Synthesis Example 7, to give 0.70 g of 2-hydroxycyclotetracosanone (quantitative yield).
Aufarbeitung
- customThe latter was subjected to a hydrogenation reaction and subsequent treatment under the same conditions as in Synthesis Example 7
Quellen und Nachweise
- ORD-Eintrag
- ord-6b50af9cd1d5494caaf2b6246d452057
- Quelldatensatz
- uspto-grants-2004_07
- Patentnummer
- US06759557B2
Verknüpfte Notizen
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