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Ammonia → N-(4-iodophenyl)1,2-diaminobenzene

HRID 1886167
ノート
印刷プレビュー

反応式

HRID 1886167 の反応式
S(S([O-])=O)([O-])=O.[Na+].[Na+].[I:9][C:10]1[CH:15]=[CH:14][C:13]([NH:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[N+:23]([O-])=O)=[CH:12][CH:11]=1.N>O.C(O)C>[I:9][C:10]1[CH:15]=[CH:14][C:13]([NH:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[NH2:23])=[CH:12][CH:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 222AmmoniaHCID 24489Sodium DithioniteHCID 15045509N-(4-iodophenyl)-2-nitroaniline

生成物 1

HCID 15045510N-(4-iodophenyl)1,2-diaminobenzene

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

According to the method of Chem. Abs., 1962, 57, 9840a, a solution of sodium dithionite (85%, 24.74 g, 121 mmol) in water (120 ml) was added to a suspension of (4-iodophenyl)-2-nitroaniline in ethanol (500 ml). The mixture was heated under reflux for 45 minutes, cooled, treated with 300 ml of dilute aqueous ammonia, and concentrated under reduced pressure. The resulting white slurry was treated with 200 ml of dilute aqueous ammonia, filtered and washed with water (200 ml). The solid was dried in a vacuum desiccator at room temperature to give N-(4-iodophenyl)1,2-diaminobenzene, 8.91 g, which gradually darkens on exposure to light, m.p. 122°-123° C.

後処理

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 45 minutes
  3. temperaturecooled
  4. concentrationconcentrated under reduced pressure
  5. additionThe resulting white slurry was treated with 200 ml of dilute aqueous ammonia
  6. filtrationfiltered
  7. washwashed with water (200 ml)
  8. customThe solid was dried in a vacuum desiccator at room temperature

出典と根拠

ORDレコード
ord-f541e1697a064118a6ca72192cf7917d
出典データセット
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05149814

反応ノート

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