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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750476Generated: November 1, 2026

Hydrochloric Acid → 2-{[5-(Trifluoromethyl)pyridin-2-yl]methylidene}cyclopentan-1-one

https://huagongshe.com/reaction/1750476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-MorpholinocyclopenteneHCID 70294—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(Trifluoromethyl)pyridine-2-carbaldehydeHCID 14422792—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-{[5-(Trifluoromethyl)pyridin-2-yl]methylidene}cyclopentan-1-oneHCID 123922717—

Reaction Steps

A solution of 5-(trifluoromethyl)pyridine-2-carbaldehyde (3.32 g, 18.96 mmol) and 4-(cyclopent-1-en-1-yl)morpholine (CAS number 936-52-7; 2.97 ml, 18.58 mmol) in toluene (50 ml) was heated to 90° C. for 18 hours. The reaction was then cooled to room temperature and concentrated HCl (2 ml) and water (2 ml) was added drop wise. The reaction was stirred at room temperature for 20 minutes and then neutralised with a saturated solution of sodium bicarbonate and then basified with 2M NaOH (aq). The organics were extracted with ethyl acetate (2×40 ml) and the combined organics were washed with brine (10 ml), dried over magnesium sulfate, filtered through a hydrophobic frit and concentrated in vacuo. The crude product was purified by column chromatography (silica, 0-20% ethyl acetate/petrol) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156829B2
Source datasetuspto-grants-2015_10
ORD IDord-d716829f9577459c95d630faea0d20e8
Source noteuspto-grants-2015_10