HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → L-prolyl-L-alanyl-L-proline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | L-prolyl-L-alanyl-L-proline benzyl ester | HCID 86749330 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | L-prolyl-L-alanyl-L-proline | HCID 9817252 | — |
Reaction Steps
Into a Parr flask flushed with argon containing 450 mg of 10% palladium on charcoal catalyst was added a solution of Ac-L-prolyl-L-alanyl-L-proline benzyl ester in (1.0 g, 2.41 mmol) absolute ethanol (100 ml). The contents were shaken under 40 psi of hydrogen overnight at room temperature. The mixture was filtered through celite and the filtrate concentrated on a rotary evaporator to give crude Ac-L-prolyl-L-alanyl-L-proline which was crystallizedfrom tetrahydrofuran-methanol-ether to give the desired product (0.57 g) in 73% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06130315 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-b0d86a19dc2f4336a83add90d6b6c58a |
| Source note | uspto-grants-2000_10 |