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Acetone → 5-Bromo-3-fluorobenzene-1,2-diamine

HRID 538130
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HRID 538130 반응식
[Br:1][C:2]1[CH:3]=[C:4]([F:12])[C:5]([N+:9]([O-])=O)=[C:6]([NH2:8])[CH:7]=1.[NH4+].[Cl-].CC(C)=O>[Zn].O>[Br:1][C:2]1[CH:7]=[C:6]([NH2:8])[C:5]([NH2:9])=[C:4]([F:12])[CH:3]=1
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참가 물질

6

반응물 3

HCID 180AcetoneHCID 25517Ammonium ChlorideHCID 669372325-Bromo-3-fluoro-2-nitroaniline

생성물 1

HCID 27732795-Bromo-3-fluorobenzene-1,2-diamine

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 962Water용매

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온도
23 °C

실험 절차

To a solution of 5-bromo-3-fluoro-2-nitro-phenylamine (2 g, 8.5 mmol), NH4Cl (6.81 g, 127.6 mmol), acetone (100 mL) and water (20 mL), was added zinc powder portion-wise (three equal portions over 5 minutes) (8.34 g, 127.6 mmol) at 0° C. The mixture was stirred for 2 h then warmed to 23° C. The mixture was filtered through Celite® and the solvents were concentrated under reduced pressure. The mixture was re-dissolved in EtOAc/DCM and filtered a second time through Celite® and the solvents were evaporated. The crude mixture was diluted with EtOAc (200 mL), washed with brine (40 mL), dried, filtered, and concentrated under reduced pressure. The resultant residue was used in the next reaction without further purification.

후처리

  1. filtrationThe mixture was filtered through Celite®
  2. concentrationthe solvents were concentrated under reduced pressure
  3. dissolutionThe mixture was re-dissolved in EtOAc/DCM
  4. filtrationfiltered a second time through Celite®
  5. customthe solvents were evaporated
  6. additionThe crude mixture was diluted with EtOAc (200 mL)
  7. washwashed with brine (40 mL)
  8. customdried
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. customThe resultant residue was used in the next reaction without further purification

출처 및 근거

ORD 기록
ord-206141e5b4e84390a1392dd276180ae9
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08865713B2

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