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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377726Generated: October 26, 2026

Methyl iodide → 4-Benzyloxy-2-methoxybenzoic acid methyl ester

https://huagongshe.com/reaction/1377726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-(benzyloxy)-2-hydroxybenzoateHCID 225489—
SolventDimethylformamideHCID 6228—
Product4-Benzyloxy-2-methoxybenzoic acid methyl esterHCID 1082603990%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 2-hydroxy-4-benzyloxybenzoate (50 g, 194 mmol) in dry DMF (500 mL) was added methyl iodide (30 mL, 2.5 eq) and the solution was cooled to 0° C. under argon. The solution was stirred at 0° C. and sodium hydride (60% dispersion in mineral oil, 12 g, 1.5 eq) was added in several portions over 15 minutes. The reaction was allowed to warm to ambient temperature with stirring over 18 hours. The reacton was quenched with 12 mL of acetic acid and the solvent was removed under reduced pressure. The residue was partitioned between methylene chloride (700 mL) and saturated sodium bicarbonate (700 mL) and the organic layer was washed with water (2×700 mL), brine, dried over MgSO4, and filtered. The solvent was removed under reduced pressure to give methyl 2-methoxy-4-benzyloxybenzoate as a crystalline solid in 90% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665719
Source datasetuspto-grants-1997_09
ORD IDord-beb6581d8b99425d8bbc2e3dd7e0ae1e
Source noteuspto-grants-1997_09