Dimethyl Sulfate → 2-Bromo-5-fluoroanisole

HRID 1822945Notes

Reaction equation

HRID 1822945 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[OH:9].[C:10](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O>CC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[O:9][CH3:10]

Participants

5

Conditions

Temperature
60 °C

Procedure

To a suspension of 2-bromo-5-fluorophenol (20.0 g, 104.7 mmol) and potassium carbonate (21.71 g, 157.1 mmol) in acetone (200 mL) was added dimethyl sulphate (10.90 mL, 115.2 mmol). The resulting suspension was allowed to stir at 60° C. for 2 h before being allowed to cool and then concentrated in vacuo. The residue was dissolved in ether (200 mL) and water (100 mL). The organic phase was washed with aqueous hydrochloric acid (2 N, 50 mL), saturated sodium bicarbonate solution (50 mL) with the resulting organic phase being dried (MgSO4) and the solvent evaporated in vacuo to give a pale yellow oil (21.46 g, 100%). δH (300 MHz, CDCl3) 7.45 (1H, dd, Ar), 6.70–6.55 (2H, m, Ar), 3.90 (3H, s, OCH3).

Workup

  1. temperatureto cool
  2. concentrationconcentrated in vacuo
  3. dissolutionThe residue was dissolved in ether (200 mL)
  4. washThe organic phase was washed with aqueous hydrochloric acid (2 N, 50 mL), saturated sodium bicarbonate solution (50 mL) with the resulting organic phase
  5. dry with materialbeing dried (MgSO4)
  6. customthe solvent evaporated in vacuo

Sources & evidence

ORD record
ord-d395f9fbe5db4762921edda7f06a24a5
Source dataset
uspto-grants-2006_05
Patent number
US07037932B2

Reaction notes

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