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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367176Generated: October 27, 2026

3,3-dimethylpyridine-2,4(1H,3H)-dione → 6-(3,5-Difluorophenyl)-3,3-dimethylpiperidine-2,4-dione

https://huagongshe.com/reaction/1367176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-dimethylpyridine-2,4(1H,3H)-dioneHCID 14198355—
ReactantHCID 178505930HCID 178505930—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
Product6-(3,5-Difluorophenyl)-3,3-dimethylpiperidine-2,4-dioneHCID 66973521—

Reaction Steps

To a solution of 3,3-dimethylpyridine-2,4(1H,3H)-dione (978 mg, 7.03 mmol) [U.S. Pat. No. 2,525,231] in benzene (10 mL) was added 3,5-difluorophenylmagnesium bromide (50 mL of a 0.5 M solution in THF, 25 mmol) and the resulting mixture was heated to reflux for 1.5 h. The mixture was cooled, quenched with 1 N aqueous HCl (10 mL), made basic with saturated NaHCO3 solution (100 mL) and extracted with EtOAc (2×150 mL). The combined organic layers were washed with H2O (50 mL), then brine (50 mL), and dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 60:40, to give the title compound. MS: m/z=254 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893079B2
Source datasetuspto-grants-2011_02
ORD IDord-32829c1b5139404391cfebb9b7f6bb40
Source noteuspto-grants-2011_02