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Hydrochloric Acid → 3-Bromo-2-chloro-4,5-difluoro-1-nitrobenzene

HRID 2232647
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HRID 2232647 반응식
[Br:1][C:2]1[C:8]([F:9])=[C:7]([F:10])[CH:6]=[C:5]([N+:11]([O-:13])=[O:12])[C:3]=1N.C(ON=O)(C)(C)C.[ClH:21]>C(#N)C>[Br:1][C:2]1[C:3]([Cl:21])=[C:5]([N+:11]([O-:13])=[O:12])[CH:6]=[C:7]([F:10])[C:8]=1[F:9]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 10906Tert-Butyl nitriteHCID 140717912-Bromo-3,4-difluoro-6-nitroaniline

생성물 1

HCID 140717923-Bromo-2-chloro-4,5-difluoro-1-nitrobenzene

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a mixture of anhydrous cupric chloride (3.1 g) and 2-bromo-3,4-difluoro-6-nitroaniline (4.6 g) in anhydrous acetonitrile (30 ml) was added t-butylnitrite (2.8 g) dropwise at 51° to 56° C. during 5 minutes. After stirring for 8 minutes at the same temperature, the reaction mixture was poured into chilled 10% diluted hydrochloric acid (30 ml) and extracted with benzene. The organic layer was washed with diluted hydrochloric acid and with water successively, dried over anhydrous sodium sulfate and concentrated. The resulting residue was purified by silica gel chromatography eluting with dichloromethane-n-hexane (1:5) to give the title compound (4.0 g).

후처리

  1. additionthe reaction mixture was poured
  2. extractionextracted with benzene
  3. washThe organic layer was washed with diluted hydrochloric acid and with water successively
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. customThe resulting residue was purified by silica gel chromatography
  7. washeluting with dichloromethane-n-hexane (1:5)

출처 및 근거

ORD 기록
ord-503409b5706a49a087dc5e93e6199ad0
출처 데이터셋
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04788320

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