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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250146Generated: October 31, 2026

Potassium Carbonate → (4-Chlorophenyl)[3-chloro-5-(trifluoromethyl)-2-pyridinyl]methanone

https://huagongshe.com/reaction/1250146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4-Chlorophenyl)-2-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]acetonitrileHCID 2773827—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product(4-Chlorophenyl)[3-chloro-5-(trifluoromethyl)-2-pyridinyl]methanoneHCID 1478937—

Reaction Conditions

Temperature23 °C

Reaction Steps

A solution of 2.0 g of 3-chloro-2-[1-(4-chlorophenyl)-1-cyanomethyl]-5-trifluoromethylpyridine (prepared by the method of Example 1) in 20 ml of dimethyl sulfoxide was admixed with a solution of 2.0 g of potassium carbonate in 3 ml of water, and the mixture was then stirred at 23° C. for 3 days under air. For work-up, the reaction mixture was poured into 200 ml of water. The product of value was then extracted with tert-butyl methyl ether (three times 80 ml). The combined organic phases were washed with water (two times 50 ml each), dried over sodium sulfate and finally concentrated. The resulting black oil was purified by Kugelrohr distillation under reduced pressure. Yield: 1.2 g (62%) of a light-yellow oil; boiling range: 110-120° C. (0.3 mbar); 1H NMR see Ex. 7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337305B1
Source datasetuspto-grants-2002_01
ORD IDord-ece2c5a3ad7245489279235f9417cc59
Source noteuspto-grants-2002_01