Ammonia → 5-Bromo-4-fluoro-2-nitroaniline

HRID 408736

Reaction equation

HRID 408736 reaction equation
[Br:1][C:2]1[CH:7]=[C:6](F)[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][C:3]=1[F:12].[NH3:13]>CO>[Br:1][C:2]1[C:3]([F:12])=[CH:4][C:5]([N+:9]([O-:11])=[O:10])=[C:6]([NH2:13])[CH:7]=1

Participants

4

Reactant 2

HCID 222AmmoniaHCID 27362864-Bromo-2,5-difluoronitrobenzene

Product 1

HCID 669372515-Bromo-4-fluoro-2-nitroaniline

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
60 °C

Procedure

A mixture of 1-bromo-2,5-difluoro-4-nitro-benzene (1.50 g, 6.30 mmol) and 7M ammonia in methanol (25 mL) was heated in a sealed tube at 60° C. for 15 h. The reaction mixture was transferred to a round bottom flask, washing the sealed tube with EtOAc. The reaction mixture was concentrated, and the crude material was used in the next step without further purification.

Workup

  1. customThe reaction mixture was transferred to a round bottom flask
  2. washwashing the sealed tube with EtOAc
  3. concentrationThe reaction mixture was concentrated
  4. customthe crude material was used in the next step without further purification

Sources & evidence

ORD record
ord-58306cd599c14be59297b4ae57f9a0c7
Source dataset
uspto-grants-2014_06
Patent number
US08759345B2

Linked notes

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