反応式
[CH3:1][C:2]1([CH3:34])[CH2:7][CH:6]([O:8][C:9](=[O:31])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([O:20][CH:21]2[CH2:26][C:25]([CH3:28])([CH3:27])[NH:24][C:23]([CH3:30])([CH3:29])[CH2:22]2)=[O:19])[CH2:5][C:4]([CH3:33])([CH3:32])[NH:3]1.[CH2:35]1[CH2:42][CH2:41][CH2:40][CH2:39][CH2:38][CH2:37][CH2:36]1.[C:43]([O:47]O)(C)([CH3:45])[CH3:44].[OH2:49]>[Mo](=O)(=O)=O>[CH:35]1([O:49][N:24]2[C:23]([CH3:30])([CH3:29])[CH2:22][CH:21]([O:20][C:18](=[O:19])[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][C:9]([O:8][CH:6]3[CH2:7][C:2]([CH3:34])([CH3:1])[N:3]([O:47][CH:43]4[CH2:45][CH2:7][CH2:6][CH2:5][CH2:4][CH2:32][CH2:44]4)[C:4]([CH3:33])([CH3:32])[CH2:5]3)=[O:31])[CH2:26][C:25]2([CH3:28])[CH3:27])[CH2:42][CH2:41][CH2:40][CH2:39][CH2:38][CH2:37][CH2:36]1参加物
6
反応条件
- 温度
- 118 °C
実験手順
A mixture of 75 g (156 mmol) of bis(2,2,6,6-tetramethylpiperidin-4-yl)sebacate, 1.3 g of molybdenum trioxide, and 475 ml of cyclooctane is heated to 118° C. To this mixture is added 130 g (1.01 mol) of 70% aq. t-butyl hydroperoxide during a 5 hour period. The reaction mixture is maintained at reflux during the addition, and water is collected in a Dean-Stark trap. The red reaction mixture is heated for 7 hours after the addition to discharge the red color. Solids are removed by filtration, and the filtrate is evaporated to give a yellow oil. Purification (Waters Prep. 500 A HPLC, 20:1 hexane: ethyl acetate) affords 78.7 g (68%) of the title compound, a colorless syrup.
後処理
- temperatureThe reaction mixture is maintained
- customis collected in a Dean-Stark trap
- customThe red reaction mixture
- temperatureis heated for 7 hours
- additionafter the addition
- customSolids are removed by filtration
- customthe filtrate is evaporated
- customto give a yellow oil
- customPurification (Waters Prep
出典と根拠
- ORDレコード
- ord-135339ad1ec14beebaec2bacd700cfd8
- 出典データセット
- uspto-grants-1993_04
- 特許番号
- US05204473
関連ノート
読み込み中…