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1-Bromo-4-nitrobenzene → 5-Bromo-2-nitroaniline

HRID 252800
Notes
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Reaction equation

HRID 252800 reaction equation
CC(C)([O-])C.[K+].[Br:7][C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][CH:9]=1.Cl.CO[NH2:20]>COCCOC.CN(C)C=O.C(OCC)(=O)C.[Cu]Cl>[Br:7][C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[C:10]([NH2:20])[CH:9]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 3

HCID 114661-Bromo-4-nitrobenzeneHCID 521874O-Methylhydroxylamine hydrochlorideHCID 23665647Potassium tert-butoxide

Product 1

HCID 53147665-Bromo-2-nitroanilineYield 75.2%

Reagents, catalysts & solvents 4

HCID 62652Cuprous chlorideCatalyst
HCID 6228
Dimethylformamide
Solvent
HCID 80711,2-DimethoxyethaneSolvent
HCID 8857Ethyl AcetateSolvent

Procedure

To a solution of potassium tert-butoxide (14.5 g; 129.2 mmol) and copper(I) chloride (301 mg; 3.04 mmol) in ethyleneglycol dimethylether (120 mL), stirred at 0° C. under nitrogen, a solution of 1-bromo-4-nitro-benzene (1, 6.141 g; 30.4 mmol) and O-methyl-hydroxylamine hydrochloride (3.174 g; 38 mmol) in N,N-dimethylformamide (65 mL) was added drop wise over 103 min, the cooling bath was removed and the mixture was allowed to react at room temperature for 3 h, diluted with ethyl acetate (600 mL) and washed with saturated aqueous ammonium chloride. The organic layer was dried (MgSO4), filtered and concentrated. After purification by flash chromatography (eluent 25% ethyl acetate in hexane), 4.96 g (75% yield) of compound 2 were obtained.

Workup

  1. customthe cooling bath was removed
  2. customto react at room temperature for 3 h
  3. washwashed with saturated aqueous ammonium chloride
  4. dry with materialThe organic layer was dried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customAfter purification by flash chromatography (eluent 25% ethyl acetate in hexane)

Sources & evidence

ORD record
ord-01c0c8d5cc37496b992f250dde29a32b
Source dataset
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07868205B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes