Dimethyl Sulfate → 3-Fluoro-2-methoxybenzaldehyde

HRID 2220293Notes

Reaction equation

HRID 2220293 reaction equation
[F:1][C:2]1[C:3]([OH:10])=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6].[C:11](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O>CC(C)=O>[F:1][C:2]1[C:3]([O:10][CH3:11])=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6]

Participants

5

Conditions

Temperature
60 °C

Procedure

To a suspension of 3-fluoro-2-hydroxybenzaldehyde (5.328 g, 38.02 mmol) and potassium carbonate (7.88 g, 57.03 mmol) in acetone (60 mL) was added dimethyl sulphate (3.96 mL, 41.83 mmol). The resulting suspension was stirred at 60° C. for 2 h before being allowed to cool and then concentrated in vacuo. The residue was dissolved in dichloromethane (100 mL) and water (50 mL). The organic phase was washed with saturated sodium bicarbonate (50 mL) with the resulting organic phase being dried (MgSO4) and the solvent evaporated in vacuo to give a pale yellow oil (6.262 g, 38.02 mmol, 100%). δH (300 MHz, CDCl3) 10.40 (1H, s, CHO), 7.60 (1H, d, Ar), 7.30 (1H, m, Ar), 7.10 (1H, m, Ar), 4.10 (3H, s, OCH3).

Workup

  1. temperatureto cool
  2. concentrationconcentrated in vacuo
  3. dissolutionThe residue was dissolved in dichloromethane (100 mL)
  4. washThe organic phase was washed with saturated sodium bicarbonate (50 mL) with the resulting organic phase
  5. dry with materialbeing dried (MgSO4)
  6. customthe solvent evaporated in vacuo

Sources & evidence

ORD record
ord-e4212303d20049d2a3a619eef1968de6
Source dataset
uspto-grants-2008_08
Patent number
US07417064B2

Reaction notes

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