HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 14003446, compound → HCID 14003453, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 14003446 | HCID 14003446 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14003453 | HCID 14003453 | 100.3% |
Reaction Steps
A solution of 8.95 g of this azide in 75 ml ethanol is hydrogenated over 2 g 10% Pd-C at 45° C. for 5 hr. The soluion is then filtered and concentrated to afford 8.3 g 3-amino-1-t-butoxycarbonylmethyl-7-phenylperhydroazepin-2-one. NMR (CDCl3, TMS): δ1.4 (s, 9H); δ1.7-2.5 (m+s, 8H); δ3.4 (d, 1H, J=17 hz); δ3.95 (d, 1H, J=17 hz); δ4.0 (broad m, 1H); δ4.95 (broad d, 1H); δ7.3 (s, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04629787 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-77c219e3d24a4c8d8c501f5f68fc6481 |
| Source note | uspto-grants-1986_12 |