Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058174Generated: October 26, 2026

2,6-Dimethoxybenzoic Acid → Benzoic acid, 2,6-dimethoxy-, methyl ester

https://huagongshe.com/reaction/1058174

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dimethoxybenzoic AcidHCID 15109—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventDimethyl CarbonateHCID 12021—
ProductBenzoic acid, 2,6-dimethoxy-, methyl esterHCID 137419—

Reaction Conditions

Temperature90 °C

Reaction Steps

1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), (836 mg, 5.49 mmol), was added to a mixture of 2,6-dimethoxybenzoic acid (1), (1.0 g, 5.49 mmol), in dimethyl carbonate (DMC) (10 mL) and the resulting mixture was heated to reflux at 90° C. for 4 hours. The reaction mixture was cooled to 25° C. and diluted with EtOAc (30 mL) and water (30 mL). The organic layer was separated and washed in sequence with 10 mL of water, 2 M HCl (2×30 mL), saturated aqueous NaHCO3 (2×30 mL) and water (2×25 mL). The organic layer was dried over Na2SO4, filtered and concentrated under vacuum to give methyl 2,6-dimethoxybenzoate (2) as a white solid. The yield of the 2,6-dimethoxybenzoate as determined by HPLC was 97-98% conversion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515167B1
Source datasetuspto-grants-2003_02
ORD IDord-107e392ba5f74beaa591bfe07c008edd
Source noteuspto-grants-2003_02