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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550814Generated: October 26, 2026

Pyridine → 1-Piperazinecarbonyl chloride, 4-[3-(trifluoromethyl)phenyl]-

https://huagongshe.com/reaction/550814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-(3-(Trifluoromethyl)phenyl)piperazineHCID 4296—
ReactantTriphosgeneHCID 94429—
SolventTetrahydrofuranHCID 8028—
Product1-Piperazinecarbonyl chloride, 4-[3-(trifluoromethyl)phenyl]-HCID 5901193679%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of triphosgene (3.2 g, 10.85 mmol) in tetrahydrofuran (10 mL) was slowly treated with pyridine (1.72 g, 21.72 mmol) via syringe. The resulting white suspension was then treated portionwise with 1-[3-(trifluoromethyl)phenyl]piperazine (500 mg, 2.17 mmol). The reaction mixture was allowed to stir at 25° C. for 18 h. At this time, the reaction was slowly quenched by the addition of water. The aqueous layer was extracted with methylene chloride. The organics were washed with a saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered and concentrated in vacuo to afford 4-(3-trifluoromethyl-phenyl)piperazine-1-carbonyl chloride (500 mg, 79%). The NMR spectrum obtained on the sample is compatible with its structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947692B2
Source datasetuspto-grants-2011_05
ORD IDord-2fcd49d7186a4f688005b1d98888c598
Source noteuspto-grants-2011_05