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4-Chloro-2-fluoro-5-isopropoxy-nitrobenzene → 4-Chloro-2-fluoro-5-isopropoxyphenylaniline

HRID 1388552
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인쇄 미리보기

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HRID 1388552 반응식
[Cl:1][C:2]1[C:7]([O:8][CH:9]([CH3:11])[CH3:10])=[CH:6][C:5]([N+:12]([O-])=O)=[C:4]([F:15])[CH:3]=1.[H][H]>C(O)C.[Pt](=O)=O>[Cl:1][C:2]1[C:7]([O:8][CH:9]([CH3:11])[CH3:10])=[CH:6][C:5]([NH:12][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[C:4]([F:15])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 131089864-Chloro-2-fluoro-5-isopropoxy-nitrobenzeneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 537633874-Chloro-2-fluoro-5-isopropoxyphenylaniline수율 69.3%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매

실험 절차

A suspension of 4-chloro-2-fluoro-5-isopropoxynitrobenzene (13.5 g) and platinum dioxide (0.4 g) in ethanol (300 ml) was subjected to catalytic reduction with hydrogen under room temperature and atmospheric pressure, whereby a designed amount of hydrogen was absorbed. The resultant mixture was filtered to remove insoluble materials, and the filtrate was concentrated. The residue was subjected to purification by silica gel chromatography to obtain 5.6 g of 4-chloro-2-fluoro-5-isopropoxyphenylaniline. nD24.5 1.5360.

후처리

  1. customatmospheric pressure, whereby a designed amount of hydrogen was absorbed
  2. filtrationThe resultant mixture was filtered
  3. customto remove insoluble materials
  4. concentrationthe filtrate was concentrated
  5. customThe residue was subjected to purification by silica gel chromatography

출처 및 근거

ORD 기록
ord-87d7f3159eb9423fa3ce616eaed7a80d
출처 데이터셋
uspto-grants-1984_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04431822

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