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Sodium Hydroxide → 3-Chloro-1H-indol-4-amine

HRID 1275673
ノート
印刷プレビュー

反応式

HRID 1275673 の反応式
[Cl:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[N+:11]([O-])=O)[NH:4][CH:3]=1.[OH-].[Na+]>C(O)C>[NH2:11][C:9]1[CH:8]=[CH:7][CH:6]=[C:5]2[C:10]=1[C:2]([Cl:1])=[CH:3][NH:4]2
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

4

反応物 2

HCID 14798Sodium HydroxideHCID 120498633-CHLORO-4-NITRO-1H-INDOLE

生成物 1

HCID 120498643-Chloro-1H-indol-4-amine収率 55%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
45 °C

実験手順

Stannous chloride (4.59 g, 20.36 mmol) is added to a solution of 3-chloro-4-nitroindole in 50 mL of ethanol. The reaction is heated to 45° C. and stirred for 1.5 hours. The reaction is cooled to room temperature and treated with 1 M aqueous sodium hydroxide solution. This mixture is extracted with ethyl acetate. The combined organic extracts are dried over magnesium sulfate, filtered and the solvents removed by rotary evaporation. The crude residue is purified via silica gel column chromatography using 15% ethyl acetate/hexanes as the eluent. The appropriate fractions are combined and the solvents removed by rotary evaporation to yield 0.466 g of 4-amino-3-chloroindole as an off-white solid (55% yield).

後処理

  1. temperatureThe reaction is cooled to room temperature
  2. extractionThis mixture is extracted with ethyl acetate
  3. dry with materialThe combined organic extracts are dried over magnesium sulfate
  4. filtrationfiltered
  5. customthe solvents removed by rotary evaporation
  6. customThe crude residue is purified via silica gel column chromatography
  7. customthe solvents removed by rotary evaporation

出典と根拠

ORDレコード
ord-fedf0ccefb104a83a82200d2df746f26
出典データセット
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06162818

反応ノート

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