反応式
[O:1]=[C:2]=[N:3][CH:4]1[CH2:13][C:12]([CH3:15])([CH3:14])[CH2:11][C:6]([CH3:16])([CH2:7][N:8]=[C:9]=[O:10])[CH2:5]1.[CH2:17]=[CH:18][CH2:19]/[CH:20]=[CH:21]\[CH2:22]/[CH:23]=[CH:24]\[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][C:32]1[CH:37]=[C:36]([OH:38])[CH:35]=[CH:34][CH:33]=1.[OH2:39].CN([CH:43]=[O:44])C>C([O-])(=O)CCCCCCCCCCC.C([O-])(=O)CCCCCCCCCCC.C([Sn+2]CCCC)CCC>[CH2:17]=[CH:18][CH2:19]/[CH:20]=[CH:21]\[CH2:22]/[CH:23]=[CH:24]\[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][C:32]1[CH:37]=[C:36]([OH:38])[CH:35]=[CH:34][CH:33]=1.[CH3:14][C:12]1([CH3:15])[CH2:11][C:6]([CH2:7][N:8]=[C:9]=[O:10])([CH3:16])[CH2:5][CH:4]([N:3]=[C:2]=[O:1])[CH2:13]1.[CH3:15][C:12]([C:13]([O:38][CH2:36][CH2:43][OH:44])=[O:39])=[CH2:14]参加物
反応条件
- 温度
- 55 °C
実験手順
Isophorone diisocyanate [IPDI] (0.73 g, 0.003 moles) in 10 ml dry DMF was taken in a 100 ml two necked flask. Cardanol (1 g, 0.0033 moles) in 10 ml DMF was added drop wise with constant stirring under nitrogen. The reaction mixture was allowed to proceed under room temperature for 1 and a half hours. Then 3 drops of dibutyl tin dilaurate [DBTDL] was added as catalyst followed by drop wise addition of 2-Hydroxy ethyl methacrylate [HEMA][0.43 g, 0.003 moles]. It was left stirring at room temperature for further 2 hours. It was then heated to 55° C. and maintained at that temperature for 2 hours. Then, the contents were poured to 150 ml water and extracted with dichloromethane. It was then washed with plenty of water and dried in vacuum oven at 60° C. for 12 hours. Yield=90% (1.95 g)
後処理
- customto proceed under room temperature for 1 and a half hours
- waitIt was left
- stirringstirring at room temperature for further 2 hours
- temperaturemaintained at that temperature for 2 hours
- extractionextracted with dichloromethane
- washIt was then washed with plenty of water
- customdried in vacuum oven at 60° C. for 12 hours
出典と根拠
- ORDレコード
- ord-510f307d6329427180adb98ea35e4565
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08048979B2
関連ノート
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