HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Oxa-5-azaspiro[3.4]octane-5-carboxylic acid, 7-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester → tert-butyl 7-amino-2-oxa-5-azaspiro[3.4]octane-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Oxa-5-azaspiro[3.4]octane-5-carboxylic acid, 7-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester | HCID 89923814 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-butyl 7-amino-2-oxa-5-azaspiro[3.4]octane-5-carboxylate | HCID 89924062 | 96.3% |
Reaction Steps
A solution of tert-butyl 7-{[(benzyloxy)carbonyl]amino}-2-oxa-5-azaspiro[3.4]octane-5-carboxylate (566 mg, 1.56 mmol) in 20 mL of MeOH was stirred with 10% Pd/C (100 mg) under hydrogen atmosphere at room temperature for 50 minutes. The resulting mixture was filtered and the filtration was concentrated in vacuo to afford tert-butyl 7-amino-2-oxa-5-azaspiro[3.4]octane-5-carboxylate (343 mg, yield: 96.3%) as light viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09206191B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-a3dfc268d2894ff79f1608cd6ff1d536 |
| Source note | uspto-grants-2015_12 |