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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644121Generated: October 29, 2026

Trifluoroacetic acid → HCID 59263044, compound

https://huagongshe.com/reaction/644121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86625836HCID 86625836—
SolventDichloromethaneHCID 6344—
ProductHCID 59263044HCID 59263044—

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 μg of 2-fluoro-4-[3-(4-piperidinyl)propoxy]benzonitrile as pale yellow oily form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700623B2
Source datasetuspto-grants-2010_04
ORD IDord-3eaf37283e464e33957361c33d9cf7a9
Source noteuspto-grants-2010_04