Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 57114913 | HCID 57114913 | — |
| Reactant | HCID 178526132 | HCID 178526132 | — |
| Solvent | Sodium Iodide | HCID 5238 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57266598 | HCID 57266598 | 70.5% |
Reaction Steps
Next, 36.4 g of thiobenzoic acid was dissolved in 300 ml of dimethylformamide and cooled on an ice bath, to which was subsequently added 10.5 g of sodium hydride. To this were added 102 g of (2S,4R)-1-(t-butoxycarbonyl)-2-ethoxycarbonyl -4-(p-toluenesulfonyloxy)pyrrolidine dissolved in 200 ml of dimethylformamide and 37.5 g of sodium iodide, followed by heating at 80° C. for 3 hours. After concentration of the reaction mixture, the thus obtained residue was dissolved in .benzene, and the resulting organic layer was washed with 5% sodium bicarbonate aqueous solution, 10% citric acid aqueous solution and water in that order, followed by drying over sodium sulfate and subsequent evaporation of the solvent under a reduced pressure. The resulting residue was purified by a silica gel column chromatography to yield 66 g of (2S,4S)-1-(t-butoxycarbonyl)-2-ethoxycarbonyl -4-benzoylthiopyrrolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05559224 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-f7b80768ff7d46eebdd05d5ea9a31630 |
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| Source note | uspto-grants-1996_09 |
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