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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856069Generated: October 30, 2026

HCID 23081330, compound → HCID 17825545, compound

https://huagongshe.com/reaction/856069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23081330HCID 23081330—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 17825545HCID 17825545100.2%

Reaction Steps

Tert-butyl 4-(4-trifluoromethylbenzyloxy)-piperidine-1-carboxylate (2.56 g, 7.12 mmol) prepared in Reference Example 122 was dissolved in methylene chloride (20 ml), to which trifluoroacetic acid (10 ml) was added dropwise, and the mixture was stirred at room temperature for 5 hours. The reaction mixture was concentrated under reduced pressure, and the residue was then dissolved in methylene chloride. This solution was neutralized with 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-trifluoromethylbenzyloxy)piperidine (1.85 g, yield 99%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-7c94c5d3849b495e9ab4c773d5cf0c10
Source noteuspto-grants-2007_08