HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632796Generated: October 30, 2026
Tributylphosphine → (3R)-3-methyl-1-(1-methyl-1H-pyrazol-3-yl)pyrrolidin-2-one
https://huagongshe.com/reaction/632796
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | Diethylazodicarboxylate toluene | HCID 66777355 | — |
| Reactant | (2R)-4-hydroxy-2-methyl-N-(1-methyl-1H-pyrazol-3-yl)butanamide | HCID 118060904 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3R)-3-methyl-1-(1-methyl-1H-pyrazol-3-yl)pyrrolidin-2-one | HCID 118061232 | 49.4% |
Reaction Steps
To a solution of (2R)-4-hydroxy-2-methyl-N-(1-methyl-1H-pyrazol-3-yl)butanamide (216 mg) and tri-n-butylphosphine (0.54 mL) in THF (10 mL) was added 40% diethyl azodicarboxylate toluene solution (1.0 mL). The reaction mixture was stirred at room temperature for 15 hr, and diluted with ethyl acetate. The diluted solution was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane), and then HPLC (C18, mobile phase: water/acetonitrile (containing 0.1% TFA)), and to the obtained fraction was added ethyl acetate. The mixture was washed with saturated aqueous sodium carbonate solution and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was concentrated under reduced pressure to give the title compound (97 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321757B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-20af8da5ff0a4a53bd11b72452bd23bf |
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| Source note | uspto-grants-2016_04 |
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