Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613192Generated: October 25, 2026

Potassium Carbonate → 2-methyl-2-[N-(3,4-methylenedioxybenzyl)-N-methylamino]propanol

https://huagongshe.com/reaction/1613192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Benzodioxole, 5-(chloromethyl)-HCID 88713—
Reactant2-Methyl-2-methylamino-1-propanolHCID 422780—
SolventAcetonitrileHCID 6342—
Product2-methyl-2-[N-(3,4-methylenedioxybenzyl)-N-methylamino]propanolHCID 5448622458%

Reaction Steps

A mixture of 2-methyl-2-methylaminopropanol (1.5 g), 3,4-methylenedioxybenzyl chloride (2.5 g) and potassium carbonate (2 g) in acetonitrile (50 ml) was heated under reflux for 4 hours and evaporated. The residue was partitioned between ether and 2M hydrochloric acid and the acidic layer was washed with methylene chloride, basified with 10% aqueous sodium carbonate solution and extracted into methylene chloride. The organic extract was dried over magnesium sulphate and evaporated to give essentially pure 2-methyl-2-[N-(3,4-methylenedioxybenzyl)-N-methylamino]propanol as a yellow oil (2.0 g, 58%) which was used directly in Example 34. A small portion of this product was dissolved in ether and the solution was treated with excess saturated ethereal hydrogen chloride and evaporated. The residue was triturated with acetone/ethyl acetate to give the title compound as a colourless solid, m.p. 157°-159°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192765
Source datasetuspto-grants-1993_03
ORD IDord-918dbfc0cb474489870cd382c91a5f79
Source noteuspto-grants-1993_03