2,6-Di-tert-butyl-4-methylphenol → HCID 19438416、化合物
反応式
Cl[P:2]1[N:5]([C:6]([CH3:9])([CH3:8])[CH3:7])[P:4](Cl)[N:3]1[C:11]([CH3:14])([CH3:13])[CH3:12].[C:15]([C:19]1[CH:24]=[C:23]([CH3:25])[CH:22]=[C:21]([C:26]([CH3:29])([CH3:28])[CH3:27])[C:20]=1[OH:30])([CH3:18])([CH3:17])[CH3:16]>C(N(CC)CC)C>[C:26]([C:21]1[CH:22]=[C:23]([CH3:25])[CH:24]=[C:19]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:20]=1[O:30][P:2]1[N:5]([C:6]([CH3:9])([CH3:8])[CH3:7])[P:4]([O:30][C:20]2[C:21]([C:26]([CH3:27])([CH3:28])[CH3:29])=[CH:22][C:23]([CH3:25])=[CH:24][C:19]=2[C:15]([CH3:18])([CH3:17])[CH3:16])[N:3]1[C:11]([CH3:14])([CH3:13])[CH3:12])([CH3:29])([CH3:28])[CH3:27]参加物
4
実験手順
The procedure of Example 1 is repeated using 2,4-dichloro-1,3-di-tert-butyl-1,3,2,4-diazadiphosphetidine, 2,6-di-tert-butyl-4-methylphenol and triethylamine to give the title compound.
出典と根拠
- ORDレコード