Acetic Acid → HCID 20300371、化合物
反応式
[NH2:1][C:2]1[O:3][CH:4]=[C:5]([C:9]([CH3:12])([CH3:11])[CH3:10])[C:6]=1[C:7]#[N:8].[C:13](O)(=[O:15])[CH3:14].C(OC(=O)C)(=O)C>>[C:13]([NH:1][C:2]1[O:3][CH:4]=[C:5]([C:9]([CH3:12])([CH3:11])[CH3:10])[C:6]=1[C:7]#[N:8])(=[O:15])[CH3:14]参加物
4
実験手順
16.4 g (0.1 mole) of 2-amino-3-cyano-4-tert.-butylfuran were heated to 100° C. with 24 ml (0.4 mole) of acetic acid and 10.4 ml (0.11 mole) of acetic anhydride for one hour. Thereafter, the reaction mixture was evaporated under reduced pressure and the residue was recrystallized from a mixture of toluene/cyclohexane (1:2). 17.2 g of 2-acetylamino-3-cyano-4-tert.-butyl-furan of melting point 135° C. were obtained in this manner.
後処理
- customThereafter, the reaction mixture was evaporated under reduced pressure
- customthe residue was recrystallized from a mixture of toluene/cyclohexane (1:2)
出典と根拠
- ORDレコード
- ord-906e8f6c272a4d838725e739580d17b5
- 出典データセット
- uspto-grants-1980_12
- 特許番号
- US04240820
反応ノート
読み込み中…