5H-Inden-5-one, 7-butyl-1,2,3,6,7,7a-hexahydro- → 5H-Inden-5-one, 7-butyloctahydro-
Reaktionsgleichung
[CH2:1]([CH:5]1[CH:13]2[C:9]([CH2:10][CH2:11][CH2:12]2)=[CH:8][C:7](=[O:14])[CH2:6]1)[CH2:2][CH2:3][CH3:4]>C(OCC)(=O)C.[Pd]>[CH2:1]([CH:5]1[CH:13]2[CH:9]([CH2:10][CH2:11][CH2:12]2)[CH2:8][C:7](=[O:14])[CH2:6]1)[CH2:2][CH2:3][CH3:4]Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
5-Butylbicyclo [4.3.0] non-1-en-3-one (120 g) is hydrogenated in ethyl acetate (125 ml) over 1.5 g of 5% palladium on carbon at a pressure of 4 atmospheres in a Parr apparatus. The solution is filtered through celite to remove the catalyst, concentrated, and the residue is vacuum distilled through a 12" Vigreaux column to yield 114 g (bp 98°-102° C. at 0.5 mm) of 5-butylbicyclo [4.3.0] nonan-3-one represented by the structure: ##STR10##
Aufarbeitung
- filtrationThe solution is filtered through celite
- customto remove the catalyst
- concentrationconcentrated
- distillationdistilled through a 12" Vigreaux column
Quellen und Nachweise
- ORD-Eintrag
- ord-306edd546c4d49ec8a9a8202f22266ad
- Quelldatensatz
- uspto-grants-1980_06
- Patentnummer
- US04206089
Notizen zur Reaktion
Wird geladen…