HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 66594811, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | 1-(4-Hydroxypiperidin-1-yl)ethan-1-one | HCID 10749291 | — |
| Reactant | HCID 66594479 | HCID 66594479 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66594811 | HCID 66594811 | 57.3% |
Reaction Steps
Diisopropylazodicarboxylate (40% in toluene, 5.7 g, 11.3 mmol) was added to a solution of (2S)-2-(4-hydroxyphenyl)-4-benzylmorpholine (2.0 g, 7.43 mmol), triphenylphosphine (3.0 g, 11.4 mmol) and 1-acetyl-4-hydroxypiperidin (1.6 g, 11.2 mmol) in tetrahydrofuran (40 ml) at room temperature and the mixture stirred for 10 hours. The mixture was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated in vacuo. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography eluting 10-50% ethyl acetate in hexane to furnish (2S)-2-(4-(1-acetylpiperidin-4-yloxy)phenyl)-4-benzylmorpholine (1.68 g, 57%) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129377B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-2aaafb3a423c4499b3a54c5d2a7f97cc |
| Source note | uspto-grants-2012_03 |