HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-butyl 4-(3-cyanophenyl)-3,6-dihydropyridine-1(2H)-carboxylate → Tert-butyl 4-(3-cyanophenyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-butyl 4-(3-cyanophenyl)-3,6-dihydropyridine-1(2H)-carboxylate | HCID 51356836 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl 4-(3-cyanophenyl)piperidine-1-carboxylate | HCID 59261051 | — |
Reaction Steps
tert-Butyl 4-(3-cyanophenyl)-3,6-dihydropyridine-1(2H)-carboxylate (1.00 g, 3.52 mmol) was combined with 20% Pd(OH)2/C (1 g) in 25 mL of methanol. This mixture was stirred under a hydrogen atmosphere using a hydrogen filled balloon for 5 h. The reaction mixture was filtered through a celite plug and the filtrate was concentrated. Purification by MPLC (silica, 38% ethyl acetate/hexanes) gave tert-butyl 4-(3-cyanophenyl)piperidine-1-carboxylate. ESI-MS calc. for C17H22N2O2: 286; Found: 309 (M+Na+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700591B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-65dd06ae8dbd43c386a29133bc3d4910 |
| Source note | uspto-grants-2010_04 |