反応式
[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]参加物
7
実験手順
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.
出典と根拠
- ORDレコード
- ord-89e4a46da6b64ab080f7764d88a2ecde
- 出典データセット
- uspto-grants-1991_02
- 特許番号
- US04990671
関連ノート
読み込み中…