HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22841886, compound → HCID 22841888, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22841886 | HCID 22841886 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22841888 | HCID 22841888 | — |
Reaction Steps
A solution of (3S,4S)-4-(1-ethoxycarbonylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone (40.0 g) in ethanol (600 ml) was hydrogenated under hydrogen atmosphere in the presence of 10% Pd/C (20.0 g) at room temperature for 3 hours. The mixture was filtered, and the filtrate was evaporated in vacuo to give (3S,4S)-4-(1-ethoxycarbonylethyl)-3-(1-(R)-hydroxyethyl)-2-azetidinone as a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112966 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-e027fb22c4214524a25a68d3777d33ff |
| Source note | uspto-grants-1992_05 |