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

HRID 1731472
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인쇄 미리보기

반응식

HRID 1731472 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, 화합물2회

생성물 1

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

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매

실험 절차

A mixture 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 at room temperature (ca. 20° C.) under 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 give 5.6 g of 4-chloro-2-fluoro-5-isopropoxyphenylaniline. nD24.5 1.5360.

후처리

  1. custom(ca. 20° C.)
  2. customwas absorbed
  3. filtrationThe resultant mixture was filtered
  4. customto remove insoluble materials
  5. concentrationthe filtrate was concentrated
  6. customThe residue was subjected to purification by silica gel chromatography

출처 및 근거

ORD 기록
ord-3fd52aa1c35a4379beaf1fd1d5042ccc
출처 데이터셋
uspto-grants-1986_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04622063

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