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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452342Generated: November 1, 2026

Water → 2-Hydroxymethyl-8-methoxy-1,4-benzodioxan

https://huagongshe.com/reaction/1452342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant8-Hydroxy-1,4-benzodioxan-2-ylmethanolHCID 14349188—
SolventDimethylformamideHCID 6228—
Product2-Hydroxymethyl-8-methoxy-1,4-benzodioxanHCID 1048810890%

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of 5.52 g of 8-hydroxy-2-hydroxymethyl-1,4-benzodioxan (prepared as described in EP 210581), 4.2g of anhydrous potassium carbonate and 2.06 ml of methyl iodide in 75 ml of anhydrous dimethylformamide was stirred at 45° C. for 8 hours. Methyl iodide (1 ml) was added to the mixture and stirring continued at the same temperature. After 8 hours, 1 ml of methyl iodide and 2.1 g of potassium carbonate were further added, and the reaction mixture was stirred at 45° C. for 6 hours. Thereafter, the mixture was cooled to room temperature, poured into water and extracted with ethyl acetate. The organic layer was washed with 6N aqueous sodium hydroxide solution, water, then dried on sodium sulfate. Evaporation of the organic layer to dryness in vacuo afforded 5.35 g of 2-hydroxymethyl-8-methoxy-1,4-benzodioxan, which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05605896
Source datasetuspto-grants-1997_02
ORD IDord-cb76fbd2c59446ce913038f001200505
Source noteuspto-grants-1997_02