Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Reactant | HCID 57239737 | HCID 57239737 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57126089 | HCID 57126089 | 74.2% |
Reaction Steps
To a solution of (2S,4R)-1-t-butoxycarbonyl-2-phthalimidomethyl-4-methanesulfonyloxypyrrolidine (3 g) in dimethylformamide (30 ml), potassium thioacetate (1.65 g) is added. The mixture is stirred at 60° C. for 3.5 hours. The reaction mixture is poured into a mixture of ethyl acetate and dilute hydrochloric acid. The organic layer is taken, washed with water, dried over sodium sulfate, and concentrated in vacuo. The residue is purified by silica gel column chromatography to give (2S,4S)-1-t-butoxycarbonyl-2-phthalimidomethyl-4-acetylthiopyrrolidine (2.12 g). Yield: 74%. Orange colored syrup. NMR δ(CDCl3) ppm: 1.30, 1.39(2×s, 9H), 1.6 to 2.0(m, 1H), 2.34(s, 3H), 2.4 to 2.67(m, 1H), 3.15 to 3.3(m, 1H), 3.65 to 4.55(m, 5H), 7.6 to to 8.0(m, 4H). IR ν (CHCl3) cm-1 : 1774, 1715, 1688.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05317016 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-1dde467375f84b3c8923bce66467af17 |
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| Source note | uspto-grants-1994_05 |
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