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

HRID 1275673
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HRID 1275673 반응식
[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
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참가 물질

4

반응물 2

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

생성물 1

HCID 120498643-Chloro-1H-indol-4-amine수율 55%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
45 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-fedf0ccefb104a83a82200d2df746f26
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06162818

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