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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856102Generated: October 29, 2026

Trifluoroacetic acid → 4-[4-(Trifluoromethoxy)phenoxy]piperidine

https://huagongshe.com/reaction/856102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 4-[4-(trifluoromethoxy)phenoxy]piperidine-1-carboxylateHCID 23081100—
SolventDichloromethaneHCID 6344—
Product4-[4-(Trifluoromethoxy)phenoxy]piperidineHCID 1611543983%

Reaction Steps

Tert-butyl 4-(4-trifluoromethoxyphenoxy)-piperidine-1-carboxylate (92 g, 254.59 mmol) prepared in Reference Example 189 was dissolved in methylene chloride (100 ml). Trifluoroacetic acid (200 ml) was added dropwise to this solution at room temperature, and the mixture was stirred overnight. The reaction mixture was concentrated under reduced pressure, and the residue was then dissolved in methylene chloride, which was neutralized with a sodium hydroxide aqueous solution. The mixture was extracted with methylene chloride. The extract was washed with brine, dried over sodium sulfate, and then filtered. The filtrate was concentrated under reduced pressure, and the residue was then purified by silica gel column chromatography (methylene chloride/methanol=5/1) to afford 4-(4-trifluoromethoxyphenoxy)piperidine (55 g, yield 83%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-48601dc8f2c84b50a540aafde8d76560
Source noteuspto-grants-2007_08