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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550853Generated: October 25, 2026

Pyridine → 4-(3-Trifluoromethyl-benzyl)-piperazine-1-carbonyl chloride

https://huagongshe.com/reaction/550853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriphosgeneHCID 94429—
Reactant1-(3-(Trifluoromethyl)benzyl)piperazineHCID 2060855—
SolventTetrahydrofuranHCID 8028—
Product4-(3-Trifluoromethyl-benzyl)-piperazine-1-carbonyl chlorideHCID 5901196092.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

A magnetically stirred mixture of triphosgene (365 mg, 1.23 mmol) in tetrahydrofuran (20 mL) under a nitrogen atmosphere was treated slowly with pyridine (485 mg, 6.15 mmol) via syringe. The resulting white suspension was then treated with a solution of 1-(3-Trifluoromethyl-benzyl) piperazine (1.0 g, 4.10 mmol) in tetrahydrofuran (10 mL) via addition funnel over 10 min. The reaction mixture was stirred at 25° C. overnight. At this time, the reaction was filtered to remove solids. The filtrate was then concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 60:40 hexanes/ethyl acetate afforded 4-(3-Trifluoromethyl-benzyl)-piperazine-1-carbonyl chloride (350 mg, 28%) as a clear oil. 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-c3155bcea5e3487984b9722812f8915f
Source noteuspto-grants-2011_05