Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765984Generated: November 1, 2026

Ethyl Acetate → (3R)-4-(2-chloroethyl)-3-(methoxymethyl)morpholine hydrochloride

https://huagongshe.com/reaction/1765984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantThionyl ChlorideHCID 24386—
Reactant2-[(3R)-3-methoxymethylmorpholino]ethanolHCID 53827486—
SolventTolueneHCID 1140—
Product(3R)-4-(2-chloroethyl)-3-(methoxymethyl)morpholine hydrochlorideHCID 69331387149.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

To an ice-cooled solution of 2-[(3R)-3-(methoxy-methyl)morpholino]ethanol (505 mg) in toluene (2.5 ml) was added dropwise a solution of thionyl chloride (429 mg) in toluene (1.5 ml) at 5° C. or below under a nitrogen atmosphere. The mixture was stirred at 70° C. for 1.5 hours. After cooling the mixture to room temperature, ethyl acetate was added to the mixture and the solvent was evaporated from the produced suspension under reduced pressure. Diisopropyl ether was added to the residue. After stirring the mixture at room temperature for 15 minutes, the produced precipitates were filtered, washed with diisopropyl ether and dried at 40° C. under reduced pressure to give (3R)-4-(2-chloroethyl)-3-(methoxymethyl)morpholine hydrochloride (620 mg) in the form of pale yellow powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07229992B2
Source datasetuspto-grants-2007_06
ORD IDord-b0681da4b5424b4ea0da8c9d843d19b5
Source noteuspto-grants-2007_06