HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 4-cyanooxane-4-carboxylate → Tert-butyl 4-(aminomethyl)oxane-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 4-cyanooxane-4-carboxylate | HCID 23131610 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl 4-(aminomethyl)oxane-4-carboxylate | HCID 67232834 | 83% |
Reaction Steps
A mixture of tert-butyl 4-cyanotetrahydro-2H-pyran-4-carboxylate (18.95 g, 0.0897 mol, step 1) and Raney Ni (1.00 g) in methanol (200 mL) was hydrogenated (3 atm) at room temperature for 12 h. Then, the mixture was filtered through a pad of Celite, and the filtrate was concentrated in vacuo to give 16.01 g (83%) of the title compound as a yellow syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705020B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-365e79b8a35040178f91116075c13185 |
| Source note | uspto-grants-2010_04 |