HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 68079399, compound → HCID 66850120, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 68079399 | HCID 68079399 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66850120 | HCID 66850120 | 96% |
Reaction Steps
Pearlman's catalyst (0.24 g) was added to an EtOH (25 ml) solution of (4aS,8aR) -tert-butyl 4-benzyldecahydroquinoxaline-1-carboxylate (2.4 g, 7.26 mmol). This suspension was stirred at room temperature for 1 hour in a hydrogen atmosphere. The catalyst was filtered through celite, and the residue was washed with EtOH. Then, the filtrate was concentrated under reduced pressure to obtain (4aS,8aR)-tert-butyl decahydroquinoxaline-1-carboxylate (1.67 g, yield: 96%) in a colorless oil form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09090572B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-540855a0120c4351a54dd5ae22d9609f |
| Source note | uspto-grants-2015_07 |