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Bromine → 2-Bromo-6-fluoro-4-nitrotoluene

HRID 1417529
Notes
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Reaction equation

HRID 1417529 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([N+:9]([O-:11])=[O:10])[CH:5]=[CH:6][C:7]=1[CH3:8].[Br:12]Br>[Fe]>[Br:12][C:6]1[CH:5]=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=[C:2]([F:1])[C:7]=1[CH3:8]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24408BromineHCID 740252-Fluoro-4-nitrotoluene

Product 1

HCID 542079842-Bromo-6-fluoro-4-nitrotolueneYield 23.2%

Reagents, catalysts & solvents 1

HCID 23925IronCatalyst

Conditions

Temperature
100 °C

Procedure

To 3-fluoro-4-methylnitrobenzene (4.0 gm, 25.8 mmol) was added bromine (5.2 gm, 32 mmol) and iron powder (100 mg). The mixture was heated under a condenser at 100° C. for 40 hr and then poured into ice water containing enough sodium sulfite to quench the excess bromine. The aqueous layer was extracted twice with ether and the ether layers were washed with brine, dried over sodium sulfate, combined and evaporated. The residue was purified by FC (10-20% ethyl acetate/hexanes) to afford 1.4 gm of the title compound as a white solid (the major and highest Rf isomer). NMR (CDCl3): δ 2.41 (d, 3H, J=3 Hz), 7.85 (dd, 1H, J=2.1 and 9 Hz), 8.24 (dd, 1H, J=1.8 and 2.1 Hz).

Workup

  1. customto quench the excess bromine
  2. extractionThe aqueous layer was extracted twice with ether
  3. washthe ether layers were washed with brine
  4. dry with materialdried over sodium sulfate
  5. customevaporated
  6. customThe residue was purified by FC (10-20% ethyl acetate/hexanes)

Sources & evidence

ORD record
ord-a24ccd3afe1d4fa38495de182ef3a319
Source dataset
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05877191

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes