反応式
[C:1]1([CH3:11])[CH:6]=[CH:5][C:4]([S:7](Cl)(=[O:9])=[O:8])=[CH:3][CH:2]=1.[Cl:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][OH:21]>N1C=CC=CC=1>[C:1]1([CH3:11])[CH:6]=[CH:5][C:4]([S:7]([O:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][Cl:12])(=[O:9])=[O:8])=[CH:3][CH:2]=1参加物
4
実験手順
p-Toluenesulphonyl chloride (20.5 g) was added to a mixture of 8-chloro-1-octanol (17.7 g) and pyridine (50 ml) of 0°. After a hour the solution was added to ice and the mixture was extracted with ether. The ethereal solution was washed with dilute hydrochloric acid, dried with magnesium sulfate, and evaporated to yield the title compound as an oil.
後処理
- additionAfter a hour the solution was added to ice
- extractionthe mixture was extracted with ether
- washThe ethereal solution was washed with dilute hydrochloric acid
- dry with materialdried with magnesium sulfate
- customevaporated
出典と根拠
- ORDレコード
- ord-b240b72b7cec4533bb47620064d06262
- 出典データセット
- uspto-grants-1985_08
- 特許番号
- US04536503
関連ノート
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