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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856035Generated: October 30, 2026

Trifluoroacetic acid → 4-(4-(Trifluoromethyl)phenoxy)piperidine

https://huagongshe.com/reaction/856035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 4-(4-(trifluoromethyl)phenoxy)piperidine-1-carboxylateHCID 22052586—
SolventDichloromethaneHCID 6344—
Product4-(4-(Trifluoromethyl)phenoxy)piperidineHCID 368839291%

Reaction Steps

Tert-butyl 4-(4-trifluoromethylphenoxy)piperidine-1-carboxylate (1.13 g, 3.27 mmol) prepared in Reference Example 37 was dissolved in methylene chloride (10 ml). To which trifluoroacetic acid (10 ml) was added dropwise and the mixture was stirred at room temperature for 5 hours. After the reaction mixture was concentrated under reduced pressure, the residue was again dissolved in methylene chloride. The solution was neutralized with a sodium hydroxide aqueous solution, and the mixture was extracted with methylene chloride. The extract was washed with brine, dried over magnesium sulfate, and then filtered. The filtrate was concentrated under reduced pressure to afford 4-(4-trifluoromethylphenoxy)piperidine (727 mg, yield 91%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-77b08985d42946d181c5e04629a6c86e
Source noteuspto-grants-2007_08