Hydrochloric Acid → 3-{[3-(Triethoxysilyl)propyl]thio}-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-1-butanone
反応式
[CH3:1]/[CH:2]=[CH:3]/[C:4]([CH:6]1[C:11]([CH3:13])([CH3:12])[CH2:10][CH2:9][CH:8]=[C:7]1[CH3:14])=[O:5].[SH:15][CH2:16][CH2:17][CH2:18][Si:19]([O:26][CH2:27][CH3:28])([O:23][CH2:24][CH3:25])[O:20][CH2:21][CH3:22].C1CCN2C(=NCCC2)CC1.Cl>C1COCC1>[CH2:21]([O:20][Si:19]([O:26][CH2:27][CH3:28])([O:23][CH2:24][CH3:25])[CH2:18][CH2:17][CH2:16][S:15][CH:2]([CH3:1])[CH2:3][C:4]([CH:6]1[C:11]([CH3:13])([CH3:12])[CH2:10][CH2:9][CH:8]=[C:7]1[CH3:14])=[O:5])[CH3:22]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 40 °C
実験手順
A solution of α-damascone (9.60 g; 50.0 mmol) and 3-mercaptopropyltriethoxysilane (95% pure, 12.52 g, 50.0 mmol) in THF (40 ml) was treated with DBU (1.52 g, 10.0 mmol) and stirred at 40° C. for 90 min. The reaction solution was treated with 5% HCl, extracted twice with ether, washed with water, saturated aqueous NaHCO3 and then with saturated aqueous NaCl, dried over Na2SO4 and concentrated at 70° C./0.01 mbar. The reaction yielded 21.2 g (99%). of crude product:
後処理
- extractionextracted twice with ether
- washwashed with water, saturated aqueous NaHCO3
- dry with materialwith saturated aqueous NaCl, dried over Na2SO4
- concentrationconcentrated at 70° C./0.01 mbar
- customThe reaction yielded 21.2 g (99%)
出典と根拠
- ORDレコード
- ord-ddfef09fcf28429baee08345b17bdbd2
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07589055B2
反応ノート
読み込み中…