HuagongsheHuagongshe Chemistry Print Report · For research reference only
N2 (benzyloxycarbonyl)-N1-tert.butyl-4(R)-hydroxy-L-prolinamide → N1-tert.butyl-4(R)-hydroxy-L-prolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N2 (benzyloxycarbonyl)-N1-tert.butyl-4(R)-hydroxy-L-prolinamide | HCID 86746270 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N1-tert.butyl-4(R)-hydroxy-L-prolinamide | HCID 57132046 | 108.6% |
Reaction Steps
0.224 g of N2 -(benzyloxycarbonyl)-N1 -tert.butyl-4(R)-hydroxy-L-prolinamide was dissolved in 20 ml of ethanol and hydrogenated over 50 mg of 10% palladium-on-carbon at room temperatureand under atmospheric pressure for 2 hours. The catalyst was filtered off and the filtrate was evaporated to give 0.13 g of N1 -tert.butyl-4(R)-hydroxy-L-prolinamide which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446161 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-deaa3f6edbe04b68b7a182eb8db2609c |
| Source note | uspto-grants-1995_08 |