HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → 4-(3-phenyl-2-((S)-2-phenylpropionyl)oxypropyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 1-Benzyl-4-(3-phenyl-2-((S)-2-phenylpropionyl)oxypropyl)piperidine | HCID 59970767 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(3-phenyl-2-((S)-2-phenylpropionyl)oxypropyl)piperidine | HCID 59970765 | — |
Reaction Steps
A solution of 0.310 g (0.7 mmol) of 1-benzyl-4-(3-phenyl-2-((S)-2-phenylpropionyl)oxypropyl)piperidine (Step 1a, isomer 1a), 0.8 g of ammonium formate, and 0.3 g of Pearlman's Catalyst (Pd(OH)2, 20% Pd, moist, Degussa type) in 20 mL of methanol was heated at reflux for 1 h. The mixture was cooled to rt and filtered through a pad of celite and concentrated to afford isomer 1b of the title compound which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06303593B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-7f13b656011640bb9238b44c6a5c82cd |
| Source note | uspto-grants-2001_10 |