HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-ethoxycarbonylpropanoyl)-L-proline tert.-butyl ester → 1-(2-ethoxycarbonylpropanoyl)-L-proline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-ethoxycarbonylpropanoyl)-L-proline tert.-butyl ester | HCID 70610337 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 1-(2-ethoxycarbonylpropanoyl)-L-proline | HCID 53678547 | — |
Reaction Steps
The ester obtained in Example 2 (5.9 g.) is dissolved in trifluoroacetic acid, the solution is kept at room temperature for one hour, and then concentrated to dryness in vacuo. The residue is dissolved in a mixture of ethyl acetate and saturated aqueous sodium bicarbonate. The aqueous phase is acidified and extracted with ethyl acetate. The ethyl acetate layer is dried over magnesium sulfate and concentrated to dryness in vacuo to obtain 1-(2-ethoxycarbonylpropanoyl)-L-proline, yield 4.1 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04128653 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-7f533fadaa4d4ac68b417529015fe1cd |
| Source note | uspto-grants-1978_12 |