HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248209Generated: October 30, 2026
Triphenylphosphine → (4S)-4-acetylthio-2-pyrrolidone
https://huagongshe.com/reaction/248209
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (R)-(+)-4-Hydroxy-2-pyrrolidinone | HCID 185505 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4S)-4-acetylthio-2-pyrrolidone | HCID 86746170 | — |
Reaction Steps
(4R)-4-Hydroxy-2-pyrrolidone (4.5 g) is suspended in tetrahydrofuran (300 ml), and thereto is added triphenylphosphine (23.4 g). After stirring the mixture for 10 minutes, diethyl azodicarboxylate (14 ml) is added dropwise to the mixture below -10° C., and the mixture is stirred at the same temperature for 10 minutes. Thioacetic acid (6.3 ml) is added dropwise to the reaction mixture below -10° C., and the mixture is stirred at the same temperature for 2 hours, and the solvent is evaporated under reduced pressure. The residue is crystallized from diisopropyl ether, and the precipitate is removed by filtration. The filtrate is concentrated under reduced pressure, and the residue is purified by silica gel column chromatography (eluent, chloroform : ethanol =98:2) to give (4S)-4-acetylthio-2-pyrrolidone (3.8 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05208348 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-f5ade569c9b14b48a955d4914a3cf2a0 |
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| Source note | uspto-grants-1993_05 |
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