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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246720Generated: October 30, 2026

Potassium Carbonate → 1-[3-(Trifluoromethyl)pyridin-2-yl]piperidin-4-one

https://huagongshe.com/reaction/1246720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
Reactant2-Chloro-3-(trifluoromethyl)pyridineHCID 589833—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
Product1-[3-(Trifluoromethyl)pyridin-2-yl]piperidin-4-oneHCID 21904751—

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Chloro-3-(trifluoromethyl)pyridine (11.92 g, 65.7 mmol)), K2CO3(19.10 g, 138 mmol), and 1,4-dioxa-8-azaspiro[4.5]decane (8.85 mL, 69.0 mmol) were combined in DMSO (65 mL) and stirred at 100° C. for 3 hours. The mixture was treated with additional 1,4-dioxa-8-azaspiro[4.5]decane (2.0 mL, 16 mmol), stirred for 2 hours, treated with additional 1,4-dioxa-8-azaspiro[4.5]decane (1.0 mL, 7.8 mmol), and stirred for 1 hour. The mixture was diluted with diethyl ether (200 mL), washed with water (250 mL), washed with brine (100 mL), dried (Na2SO4), filtered, and the filtrate was concentrated under reduced pressure. The residue was dissolved in concentrated HCl (25 mL), stirred for 3 hours, basified with concentrated NH4OH, extracted with CH2Cl2, and the phases separated. The organic phase was dried (Na2SO4), filtered, and the filtrate concentrated under reduced pressure. The residue was purified via flash chromatography (20% to 40% diethyl ether/hexanes) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129235B2
Source datasetuspto-grants-2006_10
ORD IDord-631430483e924be19e134610c3030daa
Source noteuspto-grants-2006_10