HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891582Generated: October 30, 2026
Potassium ethanethioate → HCID 58595079, compound
https://huagongshe.com/reaction/891582
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Reactant | HCID 86590854 | HCID 86590854 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58595079 | HCID 58595079 | 50% |
Reaction Steps
To a solution of (3R)-1-(4-cyano-1,3-thiazol-2-yl)-3-methanesulfonyloxypyrrolidine (300 mg, 1.10 mmol) (obtained as described in Reference Example 18(7)) in acetonitrile (9 ml) was added potassium thioacetate (376 mg, 3.30 mmol) at room temperature. The mixture was heated under reflux for 5 hours. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium hydrogencarbonate solution. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (5:1→1:1) as the eluant to afford (3S)-3-acetylthio-1-(4-cyano-1,3-thiazol-2-yl)pyrrolidine (137 mg, yield 50%) as a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001897B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-d863a3fc39904887b1a83c0fbc3a5f46 |
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| Source note | uspto-grants-2006_02 |
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