Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477812Generated: October 31, 2026

Ethanol → N,N-Dimethyl-1-(morpholin-2-yl)methanamine--hydrogen chloride (1/2)

https://huagongshe.com/reaction/477812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-(N,N-dimethylaminomethyl)-4-benzylmorpholine dihydrochlorideHCID 19834968—
CatalystHCID 178418390HCID 178418390—
SolventWaterHCID 962—
ProductN,N-Dimethyl-1-(morpholin-2-yl)methanamine--hydrogen chloride (1/2)HCID 14652585—

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-828af3ec830544b799d6ad37a30f4afe
Source noteuspto-grants-1989_12