HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Tert-butyl 4-(3-aminopropyl)-4-methylpiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | trans-4-(2-Cyanovinyl)-4-methylpiperidine-1-carboxylic acid tert-butyl ester | HCID 68857538 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Rhodium | HCID 23948 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Tert-butyl 4-(3-aminopropyl)-4-methylpiperidine-1-carboxylate | HCID 68857055 | 63.4% |
Reaction Steps
Cis/trans-4-(2-cyanovinyl)-4-methylpiperidine-1-carboxylic acid tert-butyl ester (1.00 g, 4.0 mmol), 5% Rh/Al2O3 (0.500 g) and 28% aqueous NH3 (1.25 mL) are heated at 35° C. in ethanol (20 mL) and 50 psi hydrogen gas for 18 hours. The reaction mixture is filtered through Celite®, concentrated, and chromatographed with 0-20% (2M NH3 in MeOH) in dichloromethane to give the title compound as a clear oil (0.65 g, 63% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07547691B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-8b342d06199d4a3c875f8672994238f5 |
| Source note | uspto-grants-2009_06 |