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氢氧化钠 → 3-Chloro-1H-indol-4-amine

HRID 1275673
笔记
打印预览

反应方程式

HRID 1275673 反应方程式
[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
参与物反应条件实验过程后处理来源与证据反应笔记

参与物

4

反应物 2

HCID 14798氢氧化钠HCID 120498633chloro4nitro1Hindole

产物 1

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

试剂、催化剂与溶剂 1

HCID 702乙醇溶剂

反应条件

温度
45 °C

实验过程

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).

后处理

  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

来源与证据

ORD记录
ord-fedf0ccefb104a83a82200d2df746f26
来源数据集
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
专利号
US06162818

反应笔记

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本页导航参与物反应条件实验过程后处理来源与证据反应笔记