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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
ReactantDiethylazodicarboxylate tolueneHCID 66777355—
Reactant(2R)-4-hydroxy-2-methyl-N-(1-methyl-1H-pyrazol-3-yl)butanamideHCID 118060904—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(3R)-3-methyl-1-(1-methyl-1H-pyrazol-3-yl)pyrrolidin-2-oneHCID 11806123249.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321757B2
Source datasetuspto-grants-2016_04
ORD IDord-20af8da5ff0a4a53bd11b72452bd23bf
Source noteuspto-grants-2016_04