HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 70418273, compound → HCID 70417468, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 70418273 | HCID 70418273 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70417468 | HCID 70417468 | 100.1% |
Reaction Steps
In 200 ml of methanol is suspended 3.69 g (11 mmole) of trans-1-benzyloxy-3-(tert-butoxycarbonylamino)-4-carbamoyl-2-azetidinone, and 350 mg of 10% palladium-charcoal is added to the suspension, followed by stirring under a hydrogen atmosphere at room temperature for 30 minutes. The catalyst is filtered off, and the filtrate is concentrated to dryness under reduced pressure to give 2.7 g of trans-3-(tert-butoxycarbonylamino)-4-carbamoyl-1-hydroxy-2-azetidinone as a yellowish foamy product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04794108 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-ca448b37d0ce482f901a58f30db149a5 |
| Source note | uspto-grants-1988_12 |