Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 56609827 | HCID 56609827 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86745512 | HCID 86745512 | — |
Reaction Steps
(2S,4S)-1-Methyl-2-dimethylaminocarbonyl-4-acetylthiopyrrolidine (660 mg) was dissolved in methanol (6.6 ml), and a solution of sodium methoxide (155 mg) in methanol (2.2 ml) was added thereto at room temperature under nitrogen stream, followed by stirring at the same temperature for 3 minutes. To the reaction mixture, 6N hydrochloric acid (1.05 ml) was added, and the solvent was removed by distillation. The residue was dissolved in ethanol (10.5 ml), and active carbon (99 mg) was added thereto under reflux. After refluxing for 15 minutes, the resultant mixture was filtered while hot, and the filtrate was concentrated under reduced pressure. The residue was dissolved in dichloromethane and dried over magnesium sulfate. Removal of the solvent gave (2S,4S)-1-methyl-2-dimethylaminocarbonyl-4-mercaptopyrrolidine hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05093328 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-a7f5d6da5cbf4cd0b516fae1716e1cd3 |
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| Source note | uspto-grants-1992_03 |
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