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4-Fluoro-2-methyl-6-nitroaniline → 5-Fluoro-3-methylbenzene-1,2-diamine

HRID 1953768
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인쇄 미리보기

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HRID 1953768 반응식
[F:1][C:2]1[CH:8]=[C:7]([N+:9]([O-])=O)[C:5]([NH2:6])=[C:4]([CH3:12])[CH:3]=1>O1CCCC1.[Ni]>[NH2:6][C:5]1[C:7]([NH2:9])=[CH:8][C:2]([F:1])=[CH:3][C:4]=1[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 103748424-Fluoro-2-methyl-6-nitroaniline

생성물 1

HCID 232979765-Fluoro-3-methylbenzene-1,2-diamine

시약·촉매·용매 2

HCID 935Nickel촉매HCID 8028Tetrahydrofuran용매

실험 절차

25 g (0.147 mol) of 4-fluoro-2-methyl-6-nitroaniline in 250 ml of tetrahydrofuran are hydrogenated at about 34° C. for 2 hours in the presence of 8 g of Raney nickel. The reaction mixture is then filtered off and concentrated. The title compound is obtained as a brown oil.

후처리

  1. filtrationThe reaction mixture is then filtered off
  2. concentrationconcentrated

출처 및 근거

ORD 기록
ord-6a9a47c2f2b24015a1fcf9fa351f4736
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06117873

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