HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 4-[3-(Biphenyl-2-yloxy)-propyl]-morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 2-(3-Bromo-propoxy)-biphenyl | HCID 14751946 | — |
| Product | 4-[3-(Biphenyl-2-yloxy)-propyl]-morpholine | HCID 2298326 | — |
Reaction Steps
2-(3-Bromo-propoxy)-biphenyl (1.0 g) was reacted with morpholine (5 mL) at 50° C. for 1 hour to form 4-[3-(biphenyl-2-yloxy)-propyl]-morpholine. The excess morpholine was evaporated and water was added, followed by extraction with ethyl acetate. Removal of ethyl acetate afforded 900 mg of 4-[3-(biphenyl-2-yloxy)-propyl]-morpholine (t) as an oil which was used without further purification: m/e: 297.17, MS (ES+): 298.2; 1H NMR (500 MHz, CDCl3): 7.8-7.0 (m, 9H), 4.0 (m, 2H), 3.7 (m, 4H), 2.5 (m, 6H) and 1.8 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06916798B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-c7235ded73fd44babe275470c524ad6a |
| Source note | uspto-grants-2005_07 |