HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfate Ion → N-(2-((2-hydroxy-3-(4-(2-ethoxyethoxy)-phenoxy)propyl)amino)ethyl)-4-morpholinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfate Ion | HCID 1117 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(2-Aminoethyl)-4-morpholinecarboxamide | HCID 11041198 | — |
| Reactant | 4-(2-Ethoxyethoxy)phenoxy-1,2-epoxypropane | HCID 86741206 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-((2-hydroxy-3-(4-(2-ethoxyethoxy)-phenoxy)propyl)amino)ethyl)-4-morpholinecarboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04636501 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-150ac62b6e6f4b6b966759c6249fdc88 |
| Source note | uspto-grants-1987_01 |