HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 1-[2-benzoylthio-3-methoxybutanoyl]L-proline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | 2-Bromo-3-methoxybutyryl chloride | HCID 13017047 | — |
| Reactant | HCID 178526132 | HCID 178526132 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-[2-benzoylthio-3-methoxybutanoyl]L-proline | HCID 18632466 | — |
Reaction Steps
To a solution of L-proline (5.75 g) in N sodium hydroxide (50 ml) chilled in an ice bath, 2N sodium hydroxide (25 ml) and 2-bromo-3-methoxybutyric acid chloride [obtained from 2-bromo-3-methoxybutyric acid [J. Am. Chem. Soc., 71, 1096, (1949)] and thionyl chloride] (10.7 g) are added, with vigorous stirring. After three hours, thiobenzoic acid (7.5 g) and potassium carbonate (4.8 g) are added and the mixture is stirred at room temperature overnight. The reaction mixture is acidified and extracted with ethyl acetate. The organic layer is concentrated to dryness and the residue is chromatographed on a column of silica gel with benzene-acetic acid to yield N-[2-benzoylthio-3-methoxybutanoyl]-L-proline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04745124 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-387804414a1645e685a15f0cb260fcc1 |
| Source note | uspto-grants-1988_05 |