Nitric Acid → 3,3'-Diaminobenzidine

HRID 1819972ノート

反応式

HRID 1819972 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]([C:14]2[CH:23]=[CH:22][C:17]([NH:18]C(=O)C)=[C:16]([N+:24]([O-])=O)[CH:15]=2)[CH:7]=[CH:8][C:9]=1[NH:10]C(=O)C)([O-])=O.[N+]([O-])(O)=O>C1(C2C=CC(N)=CC=2)C=CC(N)=CC=1.C(OC(=O)C)(=O)C.C(O)(=O)C>[NH2:1][C:4]1[CH:5]=[C:6]([C:14]2[CH:23]=[CH:22][C:17]([NH2:18])=[C:16]([NH2:24])[CH:15]=2)[CH:7]=[CH:8][C:9]=1[NH2:10]

参加物

6

反応物 2

HCID 944Nitric AcidHCID 44632453,3'-dinitro-N,N'-diacetylbenzidine2 回

生成物 1

HCID 70713,3'-Diaminobenzidine

試薬・触媒・溶媒 3

HCID 176Acetic Acid溶媒HCID 7111Benzidine溶媒HCID 7918Acetic Anhydride溶媒2 回

実験手順

That is, amino groups in benzidine are first protected by N-acetylation with acetic anhydride, and the resulting acetylated compound is then converted into 3,3′-dinitro-N,N′-diacetylbenzidine by nitration. For example, this nitration is performed with concentrated nitric acid in a mixture of acetic anhydride and acetic acid. 3,3′-Dinitro-N,N′-diacetylbenzidine is treated with a base to remove the acetyl groups and then treated with tin (II) chloride in hydrochloric acid to reduce the nitro groups to yield 3,3′,4,4′-tetraaminobiphenyl (Scheme 1).

後処理

  1. customto remove the acetyl groups
  2. additiontreated with tin (II) chloride in hydrochloric acid

出典と根拠

ORDレコード
ord-a0ef56b3459d450684c7015e01f86b43
出典データセット
uspto-grants-2009_10
特許番号
US07601873B2

反応ノート

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