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Hydrochloric Acid → 3,3'-Diaminobenzidine

HRID 1673070
ノート
印刷プレビュー

反応式

HRID 1673070 の反応式
O.O.Cl[Sn]Cl.Cl.[N+:7]([C:10]1[CH:11]=[C:12]([C:17]2[CH:23]=[CH:22][C:20]([NH2:21])=[C:19]([N+:24]([O-])=O)[CH:18]=2)[CH:13]=[CH:14][C:15]=1[NH2:16])([O-])=O>>[NH2:7][C:10]1[CH:11]=[C:12]([C:17]2[CH:23]=[CH:22][C:20]([NH2:21])=[C:19]([NH2:24])[CH:18]=2)[CH:13]=[CH:14][C:15]=1[NH2:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 313Hydrochloric AcidHCID 61436Stannous chloride dihydrateHCID 31067203,3'-Dinitrobenzidine

生成物 1

HCID 70713,3'-Diaminobenzidine収率 74%

実験手順

A 50 ml single neck round bottomed flask equipped with condenser, and stirring magnetic bar were placed SnCl2.2H2O (12 g, 53 mmol) and 25 ml concentrated hydrochloric acid and reaction mixture was stirred and than 3,3′-dinitrobenzidine (DNB) of formula 2 where in R═H (2.16 g, 7.9 mmol) was added in small portions over 15 minute to maintain the reaction temperature less than 60° C. The thick slurry was then stirred for additional 2 hours at 40° C. to complete the reduction. The salt of the tetramine was precipitated out, which was neutralized with cold 10% NaOH solution and the solid filtered out, washed with water dried under vacuum to give 3,3′-diaminobenzidine (DAB) in 74% yield (1.26 g).

後処理

  1. customA 50 ml single neck round bottomed flask equipped with condenser
  2. additionwas added in small portions over 15 minute
  3. temperatureto maintain the reaction temperature less than 60° C
  4. stirringThe thick slurry was then stirred for additional 2 hours at 40° C.
  5. customThe salt of the tetramine was precipitated out
  6. filtrationthe solid filtered out
  7. washwashed with water
  8. customdried under vacuum

出典と根拠

ORDレコード
ord-e26bdacde6364c4d8ee4788fdfaeda02
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07999112B2

反応ノート

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