Phenethylamine → 1-beta-Phenylethylamino-6-nitroanthraquinone
反応式
[N+:1]([C:4]1[C:17]2[C:16](=[O:18])[C:15]3[C:10](=[CH:11][C:12]([N+:19]([O-:21])=[O:20])=[CH:13][CH:14]=3)[C:9](=[O:22])[C:8]=2[CH:7]=[CH:6][CH:5]=1)([O-])=O.[C:23]1([CH2:29][CH2:30]N)[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>COCCO>[C:23]1([CH2:29][CH2:30][NH:1][C:4]2[C:17]3[C:16](=[O:18])[C:15]4[C:10](=[CH:11][C:12]([N+:19]([O-:21])=[O:20])=[CH:13][CH:14]=4)[C:9](=[O:22])[C:8]=3[CH:7]=[CH:6][CH:5]=2)[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1参加物
4
実験手順
15 g of 1,6-dinitroanthraquinone and 45 ml of β-phenylethylamine are stirred at 50° - 55° C (approx. 3 hours being required) until no further starting material is detectable. The mixture is diluted with 45 ml of ethylene glycol monomethyl ether whilst warm and the reaction product which separates out is filtered off at 50° C and rinsed with a little ethylene glycol monomethyl ether and water. 13.6 g of pure 1-β-phenylethylamino-6-nitroanthraquinone are obtained.
後処理
- temperaturewhilst warm
- filtrationthe reaction product which separates out is filtered off at 50° C
- washrinsed with a little ethylene glycol monomethyl ether and water
出典と根拠
- ORDレコード
- ord-bc2a8e225e914c9a8efa323f14c7b4ef
- 出典データセット
- uspto-grants-1976_12
- 特許番号
- US04000167
反応ノート
読み込み中…