反応式
[C:1](Cl)(=[O:11])[C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[CH:4][CH:3]=1.[CH2:13]1[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][NH:21][C:19](=[O:20])[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1>C1CCCCC1.N1C=CC=CC=1>[C:1]([N:21]1[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]1=[O:20])(=[O:11])[C:2]1[CH:10]=[CH:9][C:5]([C:6]([N:21]2[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]2=[O:20])=[O:7])=[CH:4][CH:3]=1参加物
5
実験手順
Terephthaloyl chloride (203 g, i mol) is added in the course of 30 minutes to a solution of ω-laurolactam (403 g, 2 mol) in 1600 ml of cyclohexane and 475 ml of pyridine at room temperature. The mixture is then refluxed for 3 h. After cooling, the flask contents are poured into 3 1 of ice water and the resulting light yellow precipitate is filtered off by suction and dried. Yield 498 g (95%).
後処理
- temperatureThe mixture is then refluxed for 3 h
- temperatureAfter cooling
- filtrationthe resulting light yellow precipitate is filtered off by suction
- customdried
出典と根拠
- ORDレコード
- ord-28bfdac908be45da99b312351a4086c1
- 出典データセット
- uspto-grants-1997_07
- 特許番号
- US05648521
関連ノート
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