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Ammonium Chloride → 4-Chloro-5-iodobenzene-1,2-diamine

HRID 340764
ノート
印刷プレビュー

反応式

HRID 340764 の反応式
[Cl:1][C:2]1[C:3]([I:12])=[CH:4][C:5]([N+:9]([O-])=O)=[C:6]([CH:8]=1)[NH2:7].[NH4+].[Cl-]>CCO.O.[Fe]>[Cl:1][C:2]1[CH:8]=[C:6]([NH2:7])[C:5]([NH2:9])=[CH:4][C:3]=1[I:12]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 25517Ammonium Chloride2 回HCID 223175485-Chloro-4-iodo-2-nitroaniline

生成物 1

HCID 574814674-Chloro-5-iodobenzene-1,2-diamine

試薬・触媒・溶媒 3

HCID 23925Iron触媒2 回HCID 702Ethanol溶媒HCID 962Water溶媒

反応条件

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート
温度
50 °C

実験手順

To a suspension of 5-chloro-4-iodo-2-nitroaniline (36.5 g, 122 mmol) in EtOH (800 mL) and water (150 mL) was added iron powder (38 g, 673 mmol) and NH4Cl (16 g, 306 mmol). The mixture was heated under nitrogen at 50° C. overnight. Additional iron powder (38 g, 673 mmol) and NH4Cl (16 g, 306 mmol) were added and heating was continued for 45 h. The reaction mixture was cooled, filtered and concentrated. The resulting residue was re-dissolved in ethyl acetate and washed with sodium bicarbonate solution. The organic phase was concentrated to afford the desired product as a gray solid, which was used in the next step without further purification.

後処理

  1. temperatureheating
  2. temperatureThe reaction mixture was cooled
  3. filtrationfiltered
  4. concentrationconcentrated
  5. dissolutionThe resulting residue was re-dissolved in ethyl acetate
  6. washwashed with sodium bicarbonate solution
  7. concentrationThe organic phase was concentrated

出典と根拠

ORDレコード
ord-ca4ef106e17047ae8e06ce1b93002fad
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08895596B2

反応ノート

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