反応式
[OH:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][CH2:6][NH:7]2.[CH2:12]1[CH2:18][S:15](=[O:17])(=[O:16])[O:14][CH2:13]1>C(#N)CCC>[OH:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][CH2:6][N:7]2[CH2:13][CH2:12][CH2:18][S:15]([OH:17])(=[O:16])=[O:14]参加物
4
反応条件
- 温度
- 125 °C
実験手順
A mixture of 0.8 g (5.36 mmol) of 5-hydroxy-1,2,3,4-tetrahydroquinoline and 0.5 g 1,3-propanesultone (4.1 mmol) in 12 ml of butyronitrile was heated at 125° C. for hours. The mixture was suction filtered and the filtrate evaporated under reduced pressure. The resulting off white compound crystallized. Product washed with ethyl ether and filtered of. Yield 0.8 g (80%)
後処理
- filtrationfiltered
- customthe filtrate evaporated under reduced pressure
- customThe resulting off white compound crystallized
- washProduct washed with ethyl ether
- filtrationfiltered of
出典と根拠
- ORDレコード
- ord-4f75fb939d874ca8b65e784e6f4dfb10
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08178360B2
関連ノート
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