P-Anisidine → 1-p-Anisidino-6-nitro-anthraquinone

HRID 2418994

反応式

HRID 2418994 の反応式
[N+]([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.[CH3:23][O:24][C:25]1[CH:30]=[CH:29][C:28]([NH2:31])=[CH:27][CH:26]=1>[N+](C1C=CC=CC=1)([O-])=O>[CH3:23][O:24][C:25]1[CH:30]=[CH:29][C:28]([NH:31][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:27][CH:26]=1

参加物

4

反応物 2

HCID 7732P-AnisidineHCID 741461,6-Dinitroanthraquinone

生成物 1

HCID 203164871-p-Anisidino-6-nitro-anthraquinone収率 99.6%

試薬・触媒・溶媒 1

HCID 7416Nitrobenzene溶媒

実験手順

100 g of 1,6-dinitro-anthraquinone and 84 g of p-anisidine are stirred in 300 ml of nitrobenzene at 150° C until no further starting material is detectable in a sample. The mixture is now distilled to dryness in a Venuleth apparatus under a vacuum of 5 mm and the finely ground residue is thoroughly stirred with dilute sulphuric acid, filtered off, washed until neutral and dried. 125 g of 1-p-anisidino-6-nitro-anthraquinone are obtained.

後処理

  1. distillationThe mixture is now distilled to dryness in a Venuleth apparatus under a vacuum of 5 mm
  2. filtrationfiltered off
  3. washwashed until neutral and
  4. customdried

出典と根拠

ORDレコード
ord-4884e583ea8c41fa97ffa7bbe9fd6fa7
出典データセット
uspto-grants-1978_08
特許番号
US04104284

関連ノート

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