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Stannous chloride dihydrate → 4-Bromo-3-fluorobenzene-1,2-diamine

HRID 475226
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HRID 475226 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[C:4]([N+:9]([O-])=O)[C:3]=1[F:12].O.O.Cl[Sn]Cl>CCO>[Br:1][C:2]1[C:3]([F:12])=[C:4]([NH2:9])[C:5]([NH2:8])=[CH:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 61436Stannous chloride dihydrateHCID 27831584-bromo-3-fluoro-2-nitroaniline

생성물 1

HCID 27832034-Bromo-3-fluorobenzene-1,2-diamine수율 84.7%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 140 (34 g, 0.144 mol) and EtOH (510 mL) was added SnCl2.2H2O (130.1 g, 0.576 mol) and the resulting mixture was heated to reflux for 4 h. After the completion of the reaction, the solvent was removed in vacuo. The residue was taken up in water and made slightly basic with 10% NaHCO3. The resulting solid was filtered and washed well with EtOAc. The aqueous layer was separated and extracted with EtOAc. The combined organic layers were dried (Na2SO4), filtered and concentrated in vacuo to afford 25 g (84%) of 4-bromo-3-fluoro-benzene-1,2-diamine (142) as yellow solid which was used without further purification.

후처리

  1. temperaturethe resulting mixture was heated
  2. temperatureto reflux for 4 h
  3. customAfter the completion of the reaction
  4. customthe solvent was removed in vacuo
  5. filtrationThe resulting solid was filtered
  6. washwashed well with EtOAc
  7. customThe aqueous layer was separated
  8. extractionextracted with EtOAc
  9. dry with materialThe combined organic layers were dried (Na2SO4)
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-593ca89e47be4721987adce82fd9c07d
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637537B2

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