Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980160Generated: October 30, 2026

Sulfate Ion → N-(2-((2-hydroxy-3-(4-(2-ethoxyethoxy)-phenoxy)propyl)amino)ethyl)-4-morpholinecarboxamide

https://huagongshe.com/reaction/980160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfate IonHCID 1117—
ReactantSodium HydroxideHCID 14798—
ReactantN-(2-Aminoethyl)-4-morpholinecarboxamideHCID 11041198—
Reactant4-(2-Ethoxyethoxy)phenoxy-1,2-epoxypropaneHCID 86741206—
SolventEthanolHCID 702—
ProductN-(2-((2-hydroxy-3-(4-(2-ethoxyethoxy)-phenoxy)propyl)amino)ethyl)-4-morpholinecarboxamideHCID 20222117—

Reaction Steps

12.0 g of the neutral sulphate of N-2-aminoethyl-4-morpholinecarboxamide, 2.16 g NaOH and 100 ml of absolute ethanol were refluxed 1 h. During continuing reflux 8.6 g of 3-(4-(2-ethoxyethoxy)phenoxy-1,2-epoxypropane in 50 ml of abs. ethanol was added little by little. The resulting mixture was refluxed over night, filtered and evaporated. The residue was dissolved in 200 ml of ethyl acetate and extracted twice with water. The water phase was treated with NaCl and extracted twice with ethyl acetate. The ethyl acetate phase was dried, filtered and evaporated. The residue was crystallized from ether, and recrystallized from ethyl acetate. Yield 1.1 g. Melting point 75°-77° C. (base). The structure was determined using NMR analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636501
Source datasetuspto-grants-1987_01
ORD IDord-150ac62b6e6f4b6b966759c6249fdc88
Source noteuspto-grants-1987_01