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

HRID 414378
Notes
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Reaction equation

HRID 414378 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

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).

Workup

  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)

Sources & evidence

ORD record
ord-219fa7f0beb546739c344bcd9c741062
Source dataset
uspto-grants-1988_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04791225

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes