Dimethylamine → Propanedinitrile, [amino(dimethylamino)methylene]-

HRID 616491

反応式

HRID 616491 の反応式
[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

4

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

  1. temperaturethe mixture was cooled to 0°
  2. customcondensed in a dry-ice trap
  3. additionadded to the pressure bottle
  4. customThe bottle was sealed
  5. temperaturethe reaction mixture was heated
  6. waitthe heating time was reduced to 80 minutes
  7. customyield)
  8. waitwhere it stood for two days
  9. temperatureThe pressure bottle was cooled to 0°
  10. customto attain ambient temperature
  11. customto precipitate
  12. stirringThe slurry was stirred for 30 minutes
  13. filtrationThe solid product was collected by filtration
  14. 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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