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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390767Generated: October 26, 2026

Acetone → Methyl 3-methoxy-5-methylbenzoate

https://huagongshe.com/reaction/2390767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant3-Hydroxy-5-methylbenzoic acidHCID 231756—
ProductMethyl 3-methoxy-5-methylbenzoateHCID 1383496693.5%

Reaction Steps

To acetone (180 mL) were added 3-hydroxy-5-methylbenzoic acid (9 g, 59.16 mmol), potassium carbonate (33 g, 237 mmol) and methyl iodide (37.2 mL, 591.6 mmol). For O-methylation, the resulting mixture was heated at 65° C. for 12 hours in the presence of a catalytic amount of dimethylaminopyridine. After vacuum distillation of the acetone, the concentrate was treated in water (300 mL) and dichloromethane (450 mL). The organic layer was dried over anhydrous magnesium sulfate and subjected to distillation. Column chromatography (silica gel, ethyl acetate-hexane 1:12 v/v) with the residue produced the title compound as a colorless liquid (9.98 g, 93.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273880B2
Source datasetuspto-grants-2012_09
ORD IDord-4943c0aa57844adf823ef184858acff4
Source noteuspto-grants-2012_09