HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 1-[3-(Benzoylthio)-3-(2-thenoyl)propionyl]-L-proline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-[3-bromo-3-(2-thenoyl)propionyl]-L-proline | HCID 12766095 | — |
| Reactant | HCID 178526132 | HCID 178526132 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-[3-(Benzoylthio)-3-(2-thenoyl)propionyl]-L-proline | HCID 54240767 | — |
Reaction Steps
As for Example 1, 1-[3-bromo-3-(2-thenoyl)propionyl]-L-proline (0.0085 mole) in 25 ml. of acetonitrile is added to a mixture of 0.015 mole of sodium methoxide and 0.015 mole of thiobenzoic acid in 25 ml. of acetonitrile. The mixture is stirred at room temperature for 16 hours, one ml. of acetic acid is added and the solvent removed under reduced pressure. The residue is partitioned between dichloromethane and water containing acetic acid. The organic layer is separated, washed with water, dried over magnesium sulfate and the solvent removed under reduced pressure to give the product of the Example as a pale yellow glass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04342691 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-62b10584ce5a4ee89370b916eb3eaa7c |
| Source note | uspto-grants-1982_08 |