6-Hydroxy-1,4-dimethyl-2,3,3a,4,5,6,7,8-octahydroazulene → 6-Hydroxy-1,4-dimethyl-perhydroazulene
Reaktionsgleichung
[OH:1][CH:2]1[CH2:11][CH2:10][C:9]2[CH:5]([CH2:6][CH2:7][C:8]=2[CH3:12])[CH:4]([CH3:13])[CH2:3]1>C(O)C.[Pd]>[OH:1][CH:2]1[CH2:11][CH2:10][CH:9]2[CH:5]([CH2:6][CH2:7][CH:8]2[CH3:12])[CH:4]([CH3:13])[CH2:3]1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
3.6 g of 6-hydroxy-1,4-dimethyl-2,3,3a, 4,5,6,7,8-octahydroazulene were hydrogenated in 25 ml of ethanol with 500 mg of palladium-on-carbon (10%). The reaction mixture was filtered, the filtrate evaporated and distilled under reduced pressure in a bulb-tube. There were obtained 2.5 g of 6-hydroxy-1,4-dimethyl-perhydroazulene; b.p.0.005 ca 82°; IR(film):νmax = 3360, 1460, 1375, 1030, 975 cm-1. The compound has a fresh, woody, earthy odour somewhat reminiscent of vetiver.
Aufarbeitung
- filtrationThe reaction mixture was filtered
- customthe filtrate evaporated
- distillationdistilled under reduced pressure in a bulb-tube
Quellen und Nachweise
- ORD-Eintrag
- ord-5e27d01da16a4aefa8e7e553495ba4cc
- Quelldatensatz
- uspto-grants-1977_03
- Patentnummer
- US04013711
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