Reaktionsgleichung
[OH2:1].[C:2]([C:6]1[CH:11]=[C:10]([N:12]=O)[CH:9]=[C:8]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:7]=1[OH:18])([CH3:5])([CH3:4])[CH3:3].ClCCl.[H][H].[CH3:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]>[Pd]>[OH:18][C:7]1[C:6]([C:2]([CH3:5])([CH3:4])[CH3:3])=[CH:11][C:10]([NH:12][C:24](=[O:1])[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:3][CH2:2][CH2:6][CH2:7][CH2:8][CH3:9])=[CH:9][C:8]=1[C:14]([CH3:17])([CH3:16])[CH3:15]Komponenten
7
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A 2 liter Parr bomb was charged with 210.5 g of 44.6% water wet (0.5 mole, pure, dry) 2,6-di-tert-butyl-4-nitrosophenol, 2.0 g of 5% Pd/C catalyst, 300 ml dichloromethane and 400 ml hexane. The nitrogen purged system was pressurized to 50 psi with hydrogen and the rate of hydrogen uptake noted. Hydrogenation was completed within one hour.
Quellen und Nachweise
- ORD-Eintrag
- ord-89e4a46da6b64ab080f7764d88a2ecde
- Quelldatensatz
- uspto-grants-1991_02
- Patentnummer
- US04990671
Verknüpfte Notizen
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