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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584231Generated: October 30, 2026

Methyl iodide → (3R)-3-(Methoxymethyl)-4-(phenylmethyl)morpholine

https://huagongshe.com/reaction/584231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(r)-(4-benzylmorpholin-3-yl)methanolHCID 1514271—
SolventTetrahydrofuranHCID 8028—
Product(3R)-3-(Methoxymethyl)-4-(phenylmethyl)morpholineHCID 54360669—

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of (3R)-4-benzyl-3-hydroxymethylmorpholine (0.94 g) in tetrahydrofuran (10 ml) was added dropwise to a suspension of sodium hydride (60% oil suspension, 0.22 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 (0.31 ml) was added thereto and the mixture was stirred at 40° C. for 1 hour. After cooling, the mixture was poured into ice water, and extracted with ethyl acetate. The extract was 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 (3:7) as an eluent to give (3R)-4-benzyl-3-methoxymethylmorpholine (0.88 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924278B2
Source datasetuspto-grants-2005_08
ORD IDord-e0c454a7fffd43649050f8d2af94c3a9
Source noteuspto-grants-2005_08