Methanol → 1-(1-Methyl-3-indolyl)cyclopentaneacetonitrile
反応式
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]([C:11]2([CH:16]=O)[CH2:15][CH2:14][CH2:13][CH2:12]2)=[CH:3]1.C(C1C=C(C(C)C)C=C(C(C)C)C=1S(NN)(=O)=O)(C)C.[C-:38]#[N:39].[K+].CO>O1CCCC1.O>[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]([C:11]2([CH2:16][C:38]#[N:39])[CH2:15][CH2:14][CH2:13][CH2:12]2)=[CH:3]1参加物
実験手順
2.9 g (0.0134 mol) of 1-(1-methyl-3-indolyl)-cyclopentanecarbaldehyde and 5 g (0.0166 mol) of 2,4,6-triisopropylbenzenesulphonohydrazide dissolved in 30 cm3 of tetrahydrofuran are stirred at room temperature for 3 hours. The tetrahydrofuran is thereafter evaporated off completely and 2.6 g (0.0402 mol) of potassium cyanide and 30 cm3 of methanol are added to the residue. The mixture is heated to reflux for 4.5 hours and then cooled, water is added and the mixture is extracted with dichloromethane. In succession, the organic extract obtained is washed with aqueous sodium hydrogen carbonate solution, dried over sodium sulphate and filtered and the solvent is evaporated off. The crude product thereby isolated is purified by chromatography on a silica gel column in dichloromethane and then, where appropriate, by flash chromatography using a 3:1 hexane/ethyl acetate mixture as eluent.
後処理
- customThe tetrahydrofuran is thereafter evaporated off completely
- temperatureThe mixture is heated
- temperatureto reflux for 4.5 hours
- temperaturecooled
- extractionthe mixture is extracted with dichloromethane
- extractionIn succession, the organic extract
- customobtained
- washis washed with aqueous sodium hydrogen carbonate solution
- dry with materialdried over sodium sulphate
- filtrationfiltered
- customthe solvent is evaporated off
出典と根拠
- ORDレコード
- ord-c69ebea46139456e88f2e5a007385928
- 出典データセット
- uspto-grants-1993_06
- 特許番号
- US05219859
反応ノート
読み込み中…