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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477811Generated: October 31, 2026

Dimethylamine → 2-(N,N-dimethylaminomethyl)-4-benzylmorpholine dihydrochloride

https://huagongshe.com/reaction/477811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant4-Benzyl-2-(chloromethyl)morpholineHCID 2801562—
SolventEthanolHCID 702—
Product2-(N,N-dimethylaminomethyl)-4-benzylmorpholine dihydrochlorideHCID 19834968—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 22.5 g of 4-benzyl-2-chloromethylmorpholine, 200 ml of ethanol and 200 ml of an aqueouos 26,7% dimethylamine solution is heated at 150° C. for 5 hours in an autoclave. After completion of the reaction, the solvent is distilled off under reduced pressure. After adding water, the residue is extracted with toluene three times. The extract is washed with water and dried over anhydrous magnesium sulfate. The solvent is distilled off under reduced pressure and the residue is treated with 37% hydrochloric acid-ethanol to give 2-(N,N-dimethylaminomethyl)-4-benzylmorpholine dihydrochloride as white crystals. A mixture of 22.9 g of the hydrochloride compound, 200 ml of ethanol and 100 ml of water is subjected to catalytic reduction with 2.3 g of 10% palladium-carbon at ordinary temperature and atmospheric pressure. After absorbing a theoretical volume of the hydrogen, the catalyst is filtered off and the filtrate is concentrated under reduced pressure. The obtained residue is treated with ethanol to give 2-(N,N-dimethylaminomethyl)morpholine dihydrochloride as white crystals, melting at 270°-271° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04889857
Source datasetuspto-grants-1989_12
ORD IDord-ca8414bd59c94f83badf4d6be3add441
Source noteuspto-grants-1989_12