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Methyl 2-bromo-4-fluoro-5-nitrophenoxyformate → HCID 14370869, 화합물

HRID 703696
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HRID 703696 반응식
[F:1][C:2]1[CH:7]=[C:6]([Br:8])[C:5]([O:9][C:10]([O:12][CH3:13])=[O:11])=[CH:4][C:3]=1[N+:14]([O-])=O.[H][H]>[Pt](=O)=O.C(O)C>[F:1][C:2]1[CH:7]=[C:6]([Br:8])[C:5]([O:9][C:10]([O:12][CH3:13])=[O:11])=[CH:4][C:3]=1[NH2:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 13268178Methyl 2-bromo-4-fluoro-5-nitrophenoxyformateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 14370869HCID 14370869, 화합물수율 106%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매

실험 절차

To an ethanol solution (300 ml) of 2-fluoro-4-bromo-5-methoxycarbonyloxy nitrobenzene (30.4 g, 0.1 mol) was added platinum dioxide (1.0 g) and the mixture was stirred under a hydrogen atmosphere until no hydrogen was absorbed. After the removal of the catalyst by filtration, the solvent of the filtrate was evaporated under reduced pressure to give a brown solid (28.0 g) of 2-fluoro-4-bromo-5-methoxycarbonyloxy aniline.

후처리

  1. customwas absorbed
  2. customAfter the removal of the catalyst
  3. filtrationby filtration
  4. customthe solvent of the filtrate was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-fc157a915ba443ac930c534e16c3ad6b
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04983751

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