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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272040Generated: November 1, 2026

Water → 2-(3,4-Dimethoxyphenoxy)ethanol

https://huagongshe.com/reaction/1272040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,4-DimethoxyphenolHCID 16251—
ReactantSodium hydrideHCID 24758—
Reactant2-(2-Bromoethoxy)-2H-pyranHCID 18456381—
SolventDimethylacetamideHCID 31374—
Product2-(3,4-Dimethoxyphenoxy)ethanolHCID 12298883—

Reaction Steps

A mixture of 3,4-dimethoxyphenol (155 mg, 1.0 mmol) and 60% sodium hydride (50 mg, 1.25 mmol) in DMA (6 ml) was stirred for 20 min under an atmosphere of nitrogen. 2-(2-Pyranyloxy)ethylbromide (220 mg, 1.0 mmol) was added dropwise. The reaction mixture was stirred for 6 hours at room temperature and then the mixture was poured into water (100 ml). The mixture was extracted with ethyl acetate (2×30 ml) and the combined organic extracts were dried (MgSO4). The organic phase was concentrated and the residue was dissolved in 2-propanol (30 ml) and 4 N HCl (20 ml) was added. The mixture was heated at reflux temperature for 30 min and then stirred at room temperature for 2 hours. The reaction mixture was concentrated and the residue was dissolved in ethyl acetate (50 ml). The organic solution was dried (MgSO4) and the solvent was evaporated. The oily residue was purified on silica gel (50 g) eluting with a mixture of heptane and ethyl acetate (3:2). This afforded 100 mg (50%) of 2-(3,4-dimethoxyphenoxy)ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208497B2
Source datasetuspto-grants-2007_04
ORD IDord-85e3ed54eb7c41949095337b1749c24d
Source noteuspto-grants-2007_04