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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881796Generated: November 2, 2026

Hydrochloric Acid → 2-Methoxy-4-methylbenzoic acid

https://huagongshe.com/reaction/1881796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Hydroxy-p-toluic acidHCID 5788—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
CatalystMethyl iodideHCID 6328—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
Product2-Methoxy-4-methylbenzoic acidHCID 59716424,462.6%

Reaction Steps

To a solution of 2-hydroxy-4-methylbenzoic acid (25 g, 0.164 mol) in acetone (350 mL) was added K2CO3 (68 g, 0.492 mmol) followed by MeI (41 mL, 0.656 mmol) and the reaction mixture heated at reflux for 48 hrs. After cooling to r.t. the reaction mixture was filtered and the filtrate was evaporated to give the crude methyl 2-methoxy-4-methylbenzoate. KOH (11.3 g, 1.2 eq) was dissolved in MeOH (300 mL) and the crude ester was added to the mixture and the solution heated at reflux 48 hrs. After cooling the reaction mixture was acidified with aq. HCl (1N) and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered and evaporated. The residue was triturated with Ethyl acetate/Hexane to give 20 g of 2-methoxy-4-methylbenzoic acid as a cream white solid (85% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318947B2
Source datasetuspto-grants-2012_11
ORD IDord-e23ccd826c9f48e19f6b63a957f0b187
Source noteuspto-grants-2012_11