反応式
[C:1](OC(=O)C)(=[O:3])[CH3:2].[NH2:8][C:9]1[CH:10]=[C:11]([C:15](=[O:17])[CH3:16])[CH:12]=[CH:13][CH:14]=1>C1(C)C=CC=CC=1>[C:1]([NH:8][C:9]1[CH:10]=[C:11]([C:15](=[O:17])[CH3:16])[CH:12]=[CH:13][CH:14]=1)(=[O:3])[CH3:2]参加物
4
実験手順
50 ml of acetic anhydride are added in the cold to a suspension of 30 g (0.22 mole) of 1-(3-aminophenyl)ethanone in 200 ml of toluene, and the mixture is stirred for 1 h at room temperature, then heated for 1 h to 60° C. and left to stand overnight. The precipitate obtained is drained, ground in ether and dried.
後処理
- temperatureheated for 1 h to 60° C.
- waitleft
- waitto stand overnight
- customThe precipitate obtained
- dry with materialground in ether and dried
出典と根拠
- ORDレコード
- ord-3b778f1cd77f4826ae9e52573306c1a6
- 出典データセット
- uspto-grants-1987_12
- 特許番号
- US04711899
関連ノート
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