反応式
[OH:1][C:2]1[CH:15]=[C:14]([OH:16])[CH:13]=[CH:12][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:5].[CH2:17]([O:21][CH2:22][CH2:23][CH2:24][Si:25]([O:30][CH3:31])([O:28][CH3:29])[O:26][CH3:27])[CH:18]1[O:20][CH2:19]1>[Cl-].C[N+](C)(C)C>[OH:1][C:2]1[CH:15]=[C:14]([OH:16])[CH:13]=[CH:12][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:5].[CH2:17]([O:21][CH2:22][CH2:23][CH2:24][Si:25]([O:26][CH3:27])([O:30][CH3:31])[O:28][CH3:29])[CH:18]1[O:20][CH2:19]1参加物
4
反応条件
- 温度
- 80 °C
実験手順
The above compound (Adduct I, was prepared by heating a mixture of 10.7 g (0.05 mole) of 2,4-dihydroxybenzophenone and 12.04 g (0.051 mole) of γ-glycidoxypropyltrimethoxysilane under nitrogen in the presence of 0.1 g of tetramethylammonium chloride. The mixture was stirred and gradually heated to 75°-80° C., then maintained at this temperature for 8 hours. During this period it changed into a homogeneous, viscous oil. An equivalent product was obtained when the reactants were heated at 80° C. for 4 hrs.
後処理
- temperatureby heating
- temperaturegradually heated to 75°-80° C.
- temperaturemaintained at this temperature for 8 hours
- waitDuring this period it changed
- customAn equivalent product was obtained when the reactants
出典と根拠
- ORDレコード
- ord-f4c11301f5874c448f4f5995118a4d18
- 出典データセット
- uspto-grants-1978_10
- 特許番号
- US04122233
関連ノート
読み込み中…