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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881029Generated: October 31, 2026

Trifluoroacetic acid → HCID 59263044, compound

https://huagongshe.com/reaction/881029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-[3-(4-cyano-3-fluorophenoxy)propyl]-1-piperidinecarboxylateHCID 59263029—
SolventDichloromethaneHCID 6344—
ProductHCID 59263044HCID 5926304458.6%

Reaction Steps

To a methylene chloride (5.5 mL) solution of 0.66 g of tert-butyl 4-[3-(4-cyano-3-fluorophenoxy) propyl]-1-piperidinecarboxylate was dropwise added 1.8 mL of trifluoroacetic acid under cooling with ice over a period of 2 minutes, which was then stirred at room temperature for 6 hours. The solvent was distilled off under reduced pressure, and chloroform and a 1.0 mol/L sodium hydroxide aqueous solution were added to the resultant residue. The organic layer was separated and dried with anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure. The resultant residue was purified using silica gel column chromatography (eluent; chloroform:methanol=4:1) to provide 0.28 g of 2-fluoro-4-[3-(4-piperidinyl)propoxy] benzonitrile as pale yellow oily form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993603B2
Source datasetuspto-grants-2015_03
ORD IDord-248f59dd06f84fbdbe953ce6991efe3a
Source noteuspto-grants-2015_03