Tetrahydrofuran → 4,4'-(Perfluoroisopropylidene)dicyclohexanol dimethacrylate
反応式
[F:1][C:2]([F:23])([F:22])[C:3]([CH:15]1[CH2:20][CH2:19][CH:18]([OH:21])[CH2:17][CH2:16]1)([CH:8]1[CH2:13][CH2:12][CH:11]([OH:14])[CH2:10][CH2:9]1)[C:4]([F:7])([F:6])[F:5].C(N(CC)CC)C.[O:31]1CCCC1.[C:36](Cl)(=[O:40])[C:37]([CH3:39])=[CH2:38]>O>[C:36]([OH:40])(=[O:14])[C:37]([CH3:39])=[CH2:38].[C:36]([OH:40])(=[O:31])[C:37]([CH3:39])=[CH2:38].[F:1][C:2]([F:22])([F:23])[C:3]([CH:15]1[CH2:20][CH2:19][CH:18]([OH:21])[CH2:17][CH2:16]1)([CH:8]1[CH2:9][CH2:10][CH:11]([OH:14])[CH2:12][CH2:13]1)[C:4]([F:5])([F:7])[F:6]参加物
6
実験手順
Into a reaction vessel equipped with a stirrer, thermometer and dropping funnel were placed 0.3 mole (104.4 g) of 4,4'-(perfluoroisopropylidene)dicyclohexanol, 1 mole (101.2 g) of triethylamine and 700 ml of tetrahydrofuran. To the mixture was added dropwise 1 mole (104.5 g) of methacryloyl chloride while cooling the mixture with ice. The mixture was maintained at a temperature below 20° C. for 8 hours with stirring. The reaction mixture was poured into a large excess amount of water and the resulting precipitates were recovered and washed with methanol to obtain 69 g of 4,4'-(perfluoroisopropylidene)dicyclohexanol dimethacrylate in the form of white solid.
後処理
- customInto a reaction vessel equipped with a stirrer
- temperaturewhile cooling the mixture with ice
- temperatureThe mixture was maintained at a temperature below 20° C. for 8 hours
- customthe resulting precipitates
- customwere recovered
- washwashed with methanol
出典と根拠
- ORDレコード
- ord-c5ad444026bb4f39964f67c287ddfc7b
- 出典データセット
- uspto-grants-1988_11
- 特許番号
- US04788327
反応ノート
読み込み中…