Dimethyl Sulfate → 3-Fluoro-2-methoxybenzaldehyde
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
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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
- temperatureto cool
- concentrationconcentrated in vacuo
- dissolutionThe residue was dissolved in dichloromethane (100 mL)
- washThe organic phase was washed with saturated sodium bicarbonate (50 mL) with the resulting organic phase
- dry with materialbeing dried (MgSO4)
- 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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