反応式
[CH2:1]=[C:2]1[CH2:7][CH:6]([CH3:8])[O:5][C:3]1=[O:4].C1C=CC=CC=1.[CH:15]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[CH:23]=[CH2:24])=[CH2:16]>>[CH2:1]=[C:2]1[CH2:7][CH:6]([CH3:8])[O:5][C:3]1=[O:4].[CH:15]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[CH:23]=[CH2:24])=[CH2:16]参加物
4
反応条件
- 温度
- 65 °C
実験手順
To a dry 100 mL round bottom flask equipped with a magnetic stir bar was charged 1.0153 g (8.98×10−3 mol) α-methylene-γ-valerolactone, 16.78 g (0.215 mol) benzene, 0.0561 g (4.31×10−4 mol) divinyl benzene, and 0.0067 g (4.08×10−5 mol) azobisisobutylnitrile. The reactor was purged with nitrogen for 30 minutes before heating to 65° C. The reactor was held at 65° C. for 5 hours before letting cooling the reaction mixture to room temperature and drying under vacuum.
後処理
- customTo a dry 100 mL round bottom flask equipped with a magnetic stir bar
- customThe reactor was purged with nitrogen for 30 minutes
- temperaturebefore letting cooling the reaction mixture to room temperature
- customdrying under vacuum
出典と根拠
- ORDレコード
- ord-cc45147e8cd34e0daca082f656717305
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08846817B2
関連ノート
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