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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethanol → 5-amino-6-chloro-2,3-dihydro-1H-indol-2-one

HRID 1903736
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HRID 1903736 반응식
C(O)C.[Cl-].[NH4+].[O:6]=[C:7]1[CH2:15][C:14]2[C:9](=[CH:10][C:11]([Cl:19])=[C:12]([N+:16]([O-])=O)[CH:13]=2)[NH:8]1>[Fe].O>[O:6]=[C:7]1[CH2:15][C:14]2[C:9](=[CH:10][C:11]([Cl:19])=[C:12]([NH2:16])[CH:13]=2)[NH:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 702EthanolHCID 25517Ammonium ChlorideHCID 189327986-Chloro-5-nitroindolin-2-one

생성물 1

HCID 204666645-amino-6-chloro-2,3-dihydro-1H-indol-2-one수율 93.1%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 962Water용매

실험 절차

To a mixture of ethanol (200 ml) and water (40 ml) were added ammonium chloride (2.2 g) and iron metal (19.7 g). To the mixture was added 2-oxo-5-nitro-6-chloroindoline (12.5 g) at 60° C. After refluxing for 45 minutes, the reaction mixture was filtered under warm condition. The filter cake was washed with ethanol. The combined filtrate and washings were evaporated to dryness under reduced pressure to give 2-oxo-5-amino-6-chloroindoline (10.0 g)

후처리

  1. temperatureAfter refluxing for 45 minutes
  2. filtrationthe reaction mixture was filtered
  3. temperatureunder warm condition
  4. washThe filter cake was washed with ethanol
  5. customThe combined filtrate and washings were evaporated to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-b187a0ea2d9b4cf4b0793b7d1eda6fa0
출처 데이터셋
uspto-grants-1984_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04438126

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