HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl alpha-oxobenzenebutanoate → HCID 22827210, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl alpha-oxobenzenebutanoate | HCID 562087 | — |
| Reactant | HCID 11160513 | HCID 11160513 | — |
| Reactant | HCID 22827195 | HCID 22827195 | — |
| Reactant | HCID 70443362 | HCID 70443362 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22827210 | HCID 22827210 | — |
Reaction Steps
A mixture of 0.85 grams of 1-(L-alanyl)-4-(R)-phenyl-L-proline [prepared by employing cis-4-phenyl-L-proline in the procedure of Example 2(a) to (d)], 0.2 grams of ethyl 2-oxo-4-phenylbutyrate and 1.5 grams of molecular sieves in 10 ml. of ethanol is hydrogenated under 40 psi with 1 gram of 10% palladium on carbon as the catalyst. The mixture is filtered when the uptake of hydrogen has ceased, and the filtrate is concentrated. The crude product is absorbed on an ion exchange resin (Dowex 50, H+) and eluted with 2% pyridine in water to yield the desired 1-[N-(1-(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanyl]-4-(R)-phenyl-L-proline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04462943 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-aba17faca12a40819652f298f2655515 |
| Source note | uspto-grants-1984_07 |