HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920539Generated: October 29, 2026
Methanol → 4-Benzyl-2-(4-octyloxy-phenyl)-morpholine
https://huagongshe.com/reaction/920539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Benzyl-6-(4-octyloxy-phenyl)-morpholin-3-one | HCID 67032464 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Benzyl-2-(4-octyloxy-phenyl)-morpholine | HCID 67032399 | 94.8% |
Reaction Steps
To a solution of 4-benzyl-6-(4-octyloxy-phenyl)-morpholin-3-one (22.22 g; 56.2 mmol) in THF (400 mL) was added borane-THF complex (1M, 140.4 mL; 140.4 mmol) dropwise, at 0° C. After 1 hour the mixture was allowed to warm to RT and stirred for another 2 hours. To the reaction mixture was added MeOH (30 mL), at 0° C., and the resulting mixture was stirred at RT for 30 minutes, and subsequently concentrated in vacuo. The residue was suspended in MeOH (300 mL.) and 1 M aqueous NaOH (112 mL) was added and heated under reflux for 1 hour. The resulting mixture was concentrated in vacuo and the residue was partitioned between EtOAc and 5% aqueous NaHCO3-solution. The organic layer was dried (Na2SO4), filtered, and concentrated in vacuo to afford 4-benzyl-2-(4-octyloxy-phenyl)-morpholine (20.33 g), which was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09273017B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-7620423f30514990890cf790f3572e20 |
|---|
| Source note | uspto-grants-2016_03 |
|---|