Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584230Generated: October 31, 2026

Methyl iodide → 4-Benzyl-3-methoxymethyl-3-methylmorpholine

https://huagongshe.com/reaction/584230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant(4-Benzyl-3-methylmorpholin-3-yl)methanolHCID 22342862—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Benzyl-3-methoxymethyl-3-methylmorpholineHCID 22342817—

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 4-benzyl-3-hydroxymethyl-3-methylmorpholine (1 g) in tetrahydrofuran (10 ml) was added dropwise to a suspension of sodium hydride (60% oil suspension; 0.27 g) in tetrahydrofuran (20 ml) at room temperature under nitrogen atmosphere and the whole was stirred at 70° C. for 1 hour. After cooling, methyl iodide (0.34 ml) was added to the mixture and the whole was stirred at 40° C. for 1 hour. After cooling, ethyl acetate and water were added to the mixture and the organic layer was separated, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel with a mixture of ethyl acetate and n-hexane (1:4) as an eluent to give 4-benzyl-3-methoxymethyl-3-methylmorpholine (0.77 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924278B2
Source datasetuspto-grants-2005_08
ORD IDord-40afcd7f042144a6833bddb00dee74cf
Source noteuspto-grants-2005_08