HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → L-Phenylalanyl-L-alanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1-(1(S)-t-butoxycarbonylethyl)-3(S)-azido-4(R)-phenylazetidin-2-one | HCID 13035214 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | Trifluoroacetic acid | HCID 6422 | — |
| Product | L-Phenylalanyl-L-alanine | HCID 5488196 | 94% |
Reaction Steps
After 1-(1(S)-t-butoxycarbonylethyl)-3(S)-azido-4(R)-phenylazetidin-2-one (300 mg., 0.95 mmol) was stirred in trifluoroacetic acid (2 ml.) at room temperature for 15 hours, the solvent was removed by distillation under reduced pressure. The thus obtained oil (360 mg.) was hydrogenated in 25 ml. of ethanol at 50° C. for 15 hours under ambient pressure using a 10% Pd-C (300 mg.) as a catalyst to give trifluoroacetic acid salt of L-phenylalanyl-L-alanine (311 mg., yield: 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04352752 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-8446506b615d4f04850806817179a906 |
| Source note | uspto-grants-1982_10 |