HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,7-Diphenyl-1,10-phenanthroline → Tert-butyl 4-[(vinyloxy)methyl]piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,7-Diphenyl-1,10-phenanthroline | HCID 72812 | — |
| Reactant | Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate | HCID 2764081 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Butyl vinyl ether | HCID 8108 | — |
| Product | Tert-butyl 4-[(vinyloxy)methyl]piperidine-1-carboxylate | HCID 86694316 | 9,182.5% |
Reaction Steps
4.3 g of tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate, 66 mg of 4,7-diphenyl-1,10-phenanthroline, and 45 mg of palladium acetate were added to 50 mL of butylvinyl ether, followed by stirring at room temperature for 15 minutes, and stirring at 75° C. for 2 days. The reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to obtain 4.4 g of tert-butyl 4-[(vinyloxy)methyl]piperidine-1-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822448B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-2390eb3d0a4647d3b0b617a4197dcc83 |
| Source note | uspto-grants-2014_09 |