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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427467Generated: October 30, 2026

Trifluoroacetic acid → HCID 18357113, compound

https://huagongshe.com/reaction/427467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 4-(5-cyanopyridin-2-yloxy)piperidine-1-carboxylateHCID 57027834—
SolventDichloromethaneHCID 6344—
ProductHCID 18357113HCID 1835711331.4%

Reaction Steps

To 1-(t-butyloxycarbonyl),4-(5-cyano,2-pyridinyloxy)piperidine (1.6 g) in dichloromethane (20 mL) was added trifluoroacetic acid (1.2 mL) and the reaction stirred at room temperature for 1 hour. The reaction was quenched by evaporation of trifluoroacetic acid dissolving the residue in water, basifying with sodium hydrogen carbonate and extracting the dichloromethane. The organic layer was then washed with water, brine, dried (MgSO4) and evaporated to yield 4-(5-cyano,2-pyridyloxy)piperidine as a white crystalline solid (337 mg), MS: m/z 279 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313127B1
Source datasetuspto-grants-2001_11
ORD IDord-8d9c80c641f047d8be3eeae9f4cc71c9
Source noteuspto-grants-2001_11