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Ethanol → 4-Bromo-3-fluorobenzene-1,2-diamine

HRID 1053895
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HRID 1053895 반응식
[Br:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([N+:9]([O-])=O)[C:3]=1[F:12].CCO.O.[Cl-].[NH4+]>C1COCC1.[Fe]>[Br:1][C:2]1[C:3]([F:12])=[C:4]([NH2:9])[C:5]([NH2:6])=[CH:7][CH:8]=1
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참가 물질

7

반응물 4

HCID 702EthanolHCID 962WaterHCID 25517Ammonium ChlorideHCID 27831584-bromo-3-fluoro-2-nitroaniline

생성물 1

HCID 27832034-Bromo-3-fluorobenzene-1,2-diamine수율 84%

시약·촉매·용매 2

HCID 23925Iron촉매
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
HCID 8028
Tetrahydrofuran
용매

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온도
80 °C

실험 절차

To a solution of 4-bromo-3-fluoro-2-nitroaniline (3.0 g, 12.8 mmol) in THF (30 mL) was added EtOH (30 mL) and H2O (10 mL) followed by iron powder (3.6 g, 63.8 mmol) and ammonium chloride (1.0 g, 19.2 mmol). The resulting mixture was stirred at 80° C. for 16 hours. The mixture was cooled to room temperature and filtered through diatomaceous earth. The solid was washed with EtOH until no further color came through the filter. The filtrate was concentrated in vacuo and the crude product was purified by column chromatography on silica gel using a solvent gradient of 0-40% EtOAc in hexane to give the title compound (2.2 g, 84%).

후처리

  1. temperatureThe mixture was cooled to room temperature
  2. filtrationfiltered through diatomaceous earth
  3. washThe solid was washed with EtOH until no further color
  4. concentrationThe filtrate was concentrated in vacuo
  5. customthe crude product was purified by column chromatography on silica gel using a solvent gradient of 0-40% EtOAc in hexane

출처 및 근거

ORD 기록
ord-9307c6a08fa6448c83093686af8325cf
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394279B2

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