反応式
[NH2:1][C:2]1[C:3]([CH3:9])=[CH:4][CH:5]=[CH:6][C:7]=1[CH3:8].[C:10](OC(=O)C)(=[O:12])[CH3:11].C(O)(=O)C>O>[C:10]([NH:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH3:9])(=[O:12])[CH3:11]参加物
5
実験手順
To 25 ml of 2,6-xylidine (0.20 mole) was added slowly a mixture of 25 ml of acetic anhydride (0.26 mole) and 25 ml of acetic acid (0.44 mole) under stirring at room temperature. The mixture was stirred for 30 minutes at room temperature and, then, diluted with water. The crystalline precipitate was collected by filtration to give 30.1 g (91%) of the title compound (m.p. 182°-184° C.; colorless needles).
後処理
- stirringThe mixture was stirred for 30 minutes at room temperature
- filtrationThe crystalline precipitate was collected by filtration
出典と根拠
- ORDレコード
- ord-65932ea602734fb29d525f9b6ee3ee14
- 出典データセット
- uspto-grants-1988_06
- 特許番号
- US04751232
関連ノート
読み込み中…