反応式
Cl[CH:2]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([C:11]([O:13][CH3:14])=[O:12])[C:5]=2[CH2:4][CH2:3]1.[C-:15]#[N:16].[Na+]>CS(C)=O>[C:15]([CH:2]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([C:11]([O:13][CH3:14])=[O:12])[C:5]=2[CH2:4][CH2:3]1)#[N:16]参加物
4
実験手順
In 80 ml. of dimethylsulfoxide is dissolved 15 g. of methyl 1-chloroindan-4-carboxylate and the solution is stirred. Then, 5.3 g. of sodium cyanide is added, followed by stirring for 8 hours. Following the addition of 750 ml. of water, the reaction mixture is extracted with ether. The extract is washed with a saturated aqueous solution of sodium chloride and, then, dried. The solvent is distilled off under reduced pressure and the residue is purified by column chromatography on silica gel (500 g. silica gel; eluant: chloroform). The described procedure gives methyl 1-cyanoindan-4-carboxylate as crystals melting at 76.5°-77.5° C.
後処理
- additionthe addition of 750 ml
- extractionof water, the reaction mixture is extracted with ether
- washThe extract is washed with a saturated aqueous solution of sodium chloride
- customdried
- distillationThe solvent is distilled off under reduced pressure
- customthe residue is purified by column chromatography on silica gel (500 g. silica gel; eluant: chloroform)
出典と根拠
- ORDレコード
- ord-281ea42d330a43db8ff19d08ef42a03c
- 出典データセット
- uspto-grants-1978_09
- 特許番号
- US04111997
関連ノート
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