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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922258Generated: October 25, 2026

Methyl iodide → 4-Benzyloxy-2-methoxybenzaldehyde

https://huagongshe.com/reaction/922258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Benzyloxy-2-hydroxybenzaldehydeHCID 561235—
SolventAcetonitrileHCID 6342—
Product4-Benzyloxy-2-methoxybenzaldehydeHCID 4293990100%

Reaction Steps

To a 100 mL RB flask fitted with magnetic stirrer was charged with 10 mL of acetonitrile. To the stirred solvent were added 4-(benzyloxy)-2-hydroxybenzaldehyde (1.0 g, 4.38 mmol), potassium carbonate (1.21 g, 8.76 mmol). The reaction mixture was brought to 0° C., was added methyl iodide (1.135 g, 8.76 mmol) in acetonitrile (5 mL) drop wise and stirred at room temperature for 16 h. The reaction mixture was concentrated to distill off the solvent. The residue was extracted with ethyl acetate (50 mL). The organic layer was washed with water (40 mL) and saturated brine solution (40 mL). The organic layer was dried over anhydrous Na2SO4 and the solvent was removed under reduced pressure. The product obtained as a white solid (1.06 g, yield: 100.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278915B2
Source datasetuspto-grants-2016_03
ORD IDord-7bde54a000014bf58f71b87d9aeae0e5
Source noteuspto-grants-2016_03