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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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5-Chloro-2-nitro-4-(trifluoromethoxy)aniline → 4-Chloro-5-(trifluoromethoxy)-1,2-benzenediamine

HRID 1521410
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HRID 1521410 반응식
[Cl:1][C:2]1[C:3]([O:12][C:13]([F:16])([F:15])[F:14])=[CH:4][C:5]([N+:9]([O-])=O)=[C:6]([NH2:8])[CH:7]=1>CN(C=O)C.[Pt]>[Cl:1][C:2]1[CH:7]=[C:6]([NH2:8])[C:5]([NH2:9])=[CH:4][C:3]=1[O:12][C:13]([F:16])([F:14])[F:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 265966075-Chloro-2-nitro-4-(trifluoromethoxy)aniline

생성물 1

HCID 669375074-Chloro-5-(trifluoromethoxy)-1,2-benzenediamine

시약·촉매·용매 2

HCID 23939Platinum촉매HCID 6228Dimethylformamide용매

실험 절차

5-Chloro-2-nitro-4-trifluoromethoxy-phenylamine (180 g, 0.7 mol, 1.0 equiv.) was dissolved in dry DMF (1 L) and then 5% Pt/C containing 50.2% water (4.0 g) was added. The reaction solution was hydrogenated (50 psi) at room temperature for 16 hours. HPLC analysis indicated complete reaction. MS [M+H]+ found 225.2. The reaction solution was used on the next step without isolation.

후처리

  1. customat room temperature
  2. customfor 16 hours
  3. customreaction

출처 및 근거

ORD 기록
ord-19332f96afd84f1080c8e7e184de2846
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073923B2

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