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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856139Generated: October 30, 2026

Pyridine → 4-(4-Trifluoromethylphenoxy)piperidine-1-carbonylchloride

https://huagongshe.com/reaction/856139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
ReactantTriphosgeneHCID 94429—
Reactant4-(4-(Trifluoromethyl)phenoxy)piperidineHCID 3688392—
SolventTolueneHCID 1140—
Product4-(4-Trifluoromethylphenoxy)piperidine-1-carbonylchlorideHCID 20263080272.1%

Reaction Steps

A mixture of 4-(4-trifluoromethylphenoxy) piperidine (0.6 g, 2.45 mmol), triphosgene (0.25 g, 0.86 mmol), and pyridine (0.4 ml, 4.90 mmol) in toluene (6 ml) was heated under reflux for 2.5 hours. To which ethyl acetate was added, and the mixture was washed with 10% hydrochloric acid, dried over magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure to afford 4-(4-trifluoromethylphenoxy)piperidine-1-carbonylchloride (0.72 g, yield 96%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-0e740a24c81f4925b91b2aefd186d525
Source noteuspto-grants-2007_08