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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419839Generated: October 26, 2026

Triethylamine → N-(1-Hydroxy-1-phenylpropan-2-yl)morpholine-4-carboxamide

https://huagongshe.com/reaction/2419839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(1S,2R)-2-amino-1-phenylpropan-1-olHCID 26934—
Reactant4-Morpholinecarbonyl chlorideHCID 84810—
SolventDichloromethaneHCID 6344—
ProductN-(1-Hydroxy-1-phenylpropan-2-yl)morpholine-4-carboxamideHCID 20314573—

Reaction Steps

A solution of 15.2 grams of norephedrine in 200 ml of CH2Cl2 was cooled to 0°-5° C. To this, 11.0 grams of triethylamine was added with stirring. To the stirred mixture a solution of 14.9 grams of morpholine carbonyl chloride in 10 ml of CH2Cl2 was added dropwise. The mixture was then stirred for 2 hours and left to stand at room temperature for 16 hours. The mixture was washed with water and the organic layer was dried over anhydrous sodium sulfate. The organic layer was then filtered and evaporated to a small volume. The hydroxyethylurea, N-(1-methyl-2-phenyl-2-hydroxyethyl)-4-morpholinecarboxamide was filtered off as a white solid and recrystallized from CH2Cl2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04107436
Source datasetuspto-grants-1978_08
ORD IDord-1c9c5536c525486990bb0d64c3df02aa
Source noteuspto-grants-1978_08