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4-Chloro-5-ethoxymethyl-2-fluoronitrobenzene → 4-Chloro-5-ethoxymethyl-2-fluoroaniline

HRID 231420
노트
인쇄 미리보기

반응식

HRID 231420 반응식
[Cl:1][C:2]1[C:7]([CH2:8][O:9][CH2:10][CH3:11])=[CH:6][C:5]([N+:12]([O-])=O)=[C:4]([F:15])[CH:3]=1.[H][H]>C(O)(=O)C.[Pt]>[Cl:1][C:2]1[C:7]([CH2:8][O:9][CH2:10][CH3:11])=[CH:6][C:5]([NH2:12])=[C:4]([F:15])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 145018374-Chloro-5-ethoxymethyl-2-fluoronitrobenzeneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 200323714-Chloro-5-ethoxymethyl-2-fluoroaniline

시약·촉매·용매 2

HCID 23939Platinum촉매HCID 176Acetic Acid용매

실험 절차

A solution of 4-chloro-5-ethoxymethyl-2-fluoronitrobenzene (0.9 g, 0.0039 mole) in glacial acetic acid (50 ml) was added to a 250 ml Parr bottle containing platinum IV oxide (0.3 g) under a nitrogen atmosphere. The Parr bottle was placed on a Parr hydrogenation apparatus and charged with hydrogen. The reaction mixture was allowed to shake until hydrogen absorption ceased. The catalyst was removed by vacuum filtration. The 4-chloro-5-ethoxymethyl-2-fluoroaniline produced was used in the next step in acetic acid solution without being isolated.

후처리

  1. customto shake until hydrogen absorption
  2. customThe catalyst was removed by vacuum filtration

출처 및 근거

ORD 기록
ord-3ced2f01f9b2411ea48b9ccfb74a4b1e
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04846882

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