Nitric Acid → 3-Bromo-4-nitrophenol

HRID 2423687Notes

Reaction equation

HRID 2423687 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.[N+:9]([O-:12])([OH:11])=[O:10]>C(Cl)(Cl)Cl.C(O)(=O)C>[Br:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][C:7]=1[N+:9]([O-:11])=[O:10].[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N+:9]([O-:12])=[O:10])=[C:4]([OH:8])[CH:3]=1

Participants

6

Reactant 2

HCID 944Nitric AcidHCID 115633-Bromophenol

Product 2

HCID 216473-Bromo-4-nitrophenolHCID 139704965-Bromo-2-nitrophenol

Reagents, catalysts & solvents 2

HCID 176Acetic AcidSolventHCID 6212ChloroformSolvent

Procedure

To a solution of 3-bromophenol (10 g) in chloroform (50 ml) and acetic acid (50 ml) was added 70% nitric acid (60 ml) dropwise on an ice bath, and the solution was stirred for 1 hour. The reaction mixture was poured into ice water, extracted with ethyl acetate, then sequentially washed with a saturated aqueous solution of sodium bicarbonate, water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (4.1 g) and 5-bromo-2-nitrophenol (1.8 g).

Workup

  1. extractionextracted with ethyl acetate
  2. washsequentially washed with a saturated aqueous solution of sodium bicarbonate, water and brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent was evaporated in vacuo
  5. customThe residue was purified by silica gel column chromatography (hexane-ethyl acetate system)

Sources & evidence

ORD record
ord-6b696e52957f458ba4fd67d1628ffcd7
Source dataset
uspto-grants-2011_06
Patent number
US07960412B2

Reaction notes

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