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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49691Generated: October 25, 2026

2,6-Dimethoxyphenol → 1,2,3-Trimethoxybenzene

https://huagongshe.com/reaction/49691

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DimethoxyphenolHCID 7041—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1,2,3-TrimethoxybenzeneHCID 12462—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 2,6-dimethoxyphenol (1.0 g, 6.49 mmol) in DMC (10 mL), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (0.99 g, 6.49 mmol) was added and the resulting solution was heated to reflux (90° C.) for 4.5 hours. The reaction was cooled to ambient temperature and diluted with EtOAc (50 mL) and H2O (40 mL). The organic layer was separated and washed in sequence with H2O (40 mL), 2M HCl (2×40 mL), 2M NaOH (2×40 mL) and H2O. The organic layer was dried over Na2SO4, filtered and concentrated under vacuum to give trimethoxybenzene as a solid. The yield of trimethoxybenzene as determined by HPLC was 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706929B2
Source datasetuspto-grants-2004_03
ORD IDord-74f981d105f24b61a718cb4381b6bd64
Source noteuspto-grants-2004_03