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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752240Generated: November 1, 2026

Diisopropylethylamine → (S)-3-(4-(4-methoxybenzoyl)piperidin-1-yl)pyrrolidin-2-one

https://huagongshe.com/reaction/1752240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(4-Methoxyphenyl)(piperidin-4-yl)methanoneHCID 2740588—
Reactant(R)-2-oxopyrrolidin-3-yl methanesulfonateHCID 89375789—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product(S)-3-(4-(4-methoxybenzoyl)piperidin-1-yl)pyrrolidin-2-oneHCID 7121228059.1%

Reaction Steps

To a suspension of (4-methoxyphenyl)(piperidin-4-yl)methanone (34 g, 155 mmol) and (R)-2-oxopyrrolidin-3-yl methanesulfonate (34.7 g, 194 mmol) in acetonitrile (388 mL) at room temperature was added DIPEA (108 mL, 620 mmol) and the reaction was heated to 60 C for 29 h then allowed to cool to room temperature and stirred for an additional 24 h. The reaction mixture was concentrated in vacuo to afford a waxy solid which was taken up in ethyl acetate (300 mL) and sonicated. The mixture was filtered and the resulting white solid was washed with ethyl acetate (200 mL) to yield 21.05 g. The combined filtrates were concentrated and purified via silica gel chromatography (330 g isco 0.01% NH4OH 5-10% MeOH/ethyl acetate). Pure fractions were combined, concentrated in vacuo and then taken up in ethyl acetate (80-100 mL) and stirred. A white precipitate formed that was collected by filtration. The filtrate was concentrated to a gold oil, taken up in ethyl acetate to afford a white precipitate that was collected by filtration. A total of 27.7 g of the title material was obtained as a white solid. Calculated MS=302.4. found MS (ESI) m/e 303.4 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163003B2
Source datasetuspto-grants-2015_10
ORD IDord-49817b6c0273432e91eb3924e7fd2e1b
Source noteuspto-grants-2015_10