反応式
[NH2:1][C:2](SC)=[C:3]([C:6]#[N:7])[C:4]#[N:5].[CH3:10][NH:11][CH3:12]>CN(C)C=O>[NH2:1][C:2]([N:11]([CH3:12])[CH3:10])=[C:3]([C:6]#[N:7])[C:4]#[N:5]参加物
実験手順
Into a pressure bottle were placed 5.6 g of 3-amino-2-cyano-3-(methylthio)propenenitrile and 3 ml of dimethylformamide, and the mixture was cooled to 0°. A volume of 5.4 ml (3.6 g) of dimethylamine was condensed in a dry-ice trap and added to the pressure bottle. The bottle was sealed and the reaction mixture was heated, with stirring, at 100° for 3-4 hours (in subsequent runs, the heating time was reduced to 80 minutes without reducing the yield). After this time, the mixture was allowed to cool to ambient temperature, where it stood for two days. The pressure bottle was cooled to 0° and opened. The mixture was allowed to attain ambient temperature, then was poured into 300 ml of ice-water, causing a white solid to precipitate. The slurry was stirred for 30 minutes. The solid product was collected by filtration and washed with cold water to give 5.1 g of 3-amino-2-cyano-3-(dimethylamino)propenenitrile, m.p. 228°-229°. The nmr was consistent with the assigned structure.
後処理
- temperaturethe mixture was cooled to 0°
- customcondensed in a dry-ice trap
- additionadded to the pressure bottle
- customThe bottle was sealed
- temperaturethe reaction mixture was heated
- waitthe heating time was reduced to 80 minutes
- customyield)
- waitwhere it stood for two days
- temperatureThe pressure bottle was cooled to 0°
- customto attain ambient temperature
- customto precipitate
- stirringThe slurry was stirred for 30 minutes
- filtrationThe solid product was collected by filtration
- washwashed with cold water
出典と根拠
- ORDレコード
- ord-9b827413de50471ca2d08d68b713446e
- 出典データセット
- uspto-grants-1978_02
- 特許番号
- US04075001
関連ノート
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