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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N1-isopropyl-4-chloro-2-nitroaniline → HCID 19437878, 화합물

HRID 1734546
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HRID 1734546 반응식
[Cl:1][C:2]1[CH:11]=[CH:10][C:5]([NH:6][CH:7]([CH3:9])[CH3:8])=[C:4]([N+:12]([O-])=O)[CH:3]=1.[N+:15]([O-:18])(O)=[O:16].[C:19](OC(=O)C)(=[O:21])C>C(OC(=O)C)(=O)C>[Cl:1][C:2]1[C:11]([N+:15]([O-:18])=[O:16])=[CH:10][C:5]2[N:6]([CH:7]([CH3:8])[CH3:9])[C:19](=[O:21])[NH:12][C:4]=2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2736692N1-isopropyl-4-chloro-2-nitroanilineHCID 22241977HCID 22241977, 화합물

생성물 1

HCID 19437878HCID 19437878, 화합물수율 80%

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

The compound of Example 4 (1.0 g, 5.0 mmol) was suspended in acetic anhydride (10 mL) and cooled in an ice bath. To this mixture was added dropwise 1.5 mL of a 1:2 mixture of nitric acid/acetic anhydride. The reaction mixture was stirred for 5 minutes before being poured into ice-water. The solid was filtered and washed well with water and suction-dried to afford 1.01 g (80%) of the title compound as a solid.

후처리

  1. temperaturecooled in an ice bath
  2. additionTo this mixture was added dropwise
  3. filtrationThe solid was filtered
  4. washwashed well with water
  5. customsuction-dried

출처 및 근거

ORD 기록
ord-5de67d1ef5bd48728f22d935007e5fa6
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05534521

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