HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371387Generated: October 30, 2026
Triphenylphosphine → HCID 56609827, compound
https://huagongshe.com/reaction/2371387
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (2S,4R)-4-hydroxy-N,N,1-trimethylpyrrolidine-2-carboxamide | HCID 45116063 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 56609827 | HCID 56609827 | — |
Reaction Steps
(2S,4R)-1-Methyl-2-dimethylaminocarbonyl-4-hydroxypyrrolidine (970 mg) was dissolved in dry tetrahydrofuran (11.1 ml), and triphenylphosphine (2.66 g) was added thereto. To the resultant mixture, diethyl azodicarboxylate (1.60 ml) was added under nitrogen steam while ice-cooling, and the mixture was stirred for 30 minutes. Thioacetic acid (1.45 ml) was added to the mixture under ice-cooling, and stirring was continued for 40 minutes under ice-cooling, followed by allowing to stand overnight. The reaction mixture was diluted with dichloromethane, washed with aqueous potassium carbonate solution and dried over magnesium sulfate. After removal of the solvent by distillation, the residue was purified by silica gel column chromatography to give (2S,4S)-1-methyl-2-dimethylaminocarbonyl-4-acetylthiopyrrolidine.
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-acd768fa2c424d1c8e89b38b2b0efafe |
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| Source note | uspto-grants-1992_03 |
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