反応式
O[CH2:2][CH2:3][C:4]([NH2:6])=[O:5].[CH2:7](N)[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].C(C1C(O)=C(C(C)(C)C)C=C(C)C=1)(C)(C)C.N>>[CH2:18]([NH:6][C:4](=[O:5])[CH:3]=[CH2:2])[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH3:7]参加物
5
反応条件
- 温度
- 160 °C
実験手順
82 g of β-hydroxypropionamide and 195 g of dodecylamine were heated with 50 mg of 2,6-di-t-butyl-p-cresol for 4 hours in a temperature range of 130° C. to 190° C. unitl the evolution of ammonia was complete. After adding 5 g of polyphosphoric acid the reaction mixture was maintained at 160° C. for 1 hour and then distilled in an oil pump vacuum. The main run was taken off between 148° C. and 168° C. at 0.3 bar and crystallized in the receiver.
後処理
- distillationdistilled in an oil pump vacuum
- customwas taken off between 148° C. and 168° C. at 0.3 bar
- customcrystallized in the receiver
出典と根拠
- ORDレコード
- ord-b0cebc79842c4d31bd041756cf527308
- 出典データセット
- uspto-grants-1980_12
- 特許番号
- US04237067
関連ノート
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