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Stannous Chloride → 4-Bromo-5-fluoro-1,2-benzenediamine

HRID 475210
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HRID 475210 반응식
[Br:1][C:2]1[C:8]([F:9])=[CH:7][C:5]([NH2:6])=[C:4]([N+:10]([O-])=O)[CH:3]=1.Cl[Sn]Cl>CCO>[Br:1][C:2]1[CH:3]=[C:4]([NH2:10])[C:5]([NH2:6])=[CH:7][C:8]=1[F:9]
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참가 물질

4

반응물 2

HCID 24479Stannous ChlorideHCID 219119284-Bromo-5-fluoro-2-nitroaniline

생성물 1

HCID 199585604-Bromo-5-fluoro-1,2-benzenediamine수율 43.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a suspension of 96 (1.57 g, 6.74 mmol) in EtOH (16 mL) was added SnCl2 (3.82 g, 20.2 mmol). The reaction mixture was heated at reflux for 14 h, cooled to RT and concentrated in vacuo. The residue was partitioned between EtOAc (100 mL) and sat'd. aq. NaHCO3 (200 mL). The resulting slurry was filtered through a pad of Celite® and the wet cake was washed with EtOAc (3×50 mL). The organic layer was washed sequentially with saturated NaHCO3, water, and brine, dried (MgSO4), filtered and concentrated in vacuo to afford 600 mg (43%) of 4-bromo-5-fluorobenzene-1,2-diamine (98) as yellow solid: MS (ESI) m/z=205 [M+1]+.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 14 h
  3. concentrationconcentrated in vacuo
  4. customThe residue was partitioned between EtOAc (100 mL)
  5. filtrationThe resulting slurry was filtered through a pad of Celite®
  6. washthe wet cake was washed with EtOAc (3×50 mL)
  7. washThe organic layer was washed sequentially with saturated NaHCO3, water, and brine
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-7a9c016805e44a2d9e54cc9d32800f67
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637537B2

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