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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856034Generated: October 30, 2026

Tributylphosphine → tert-Butyl 4-(4-(trifluoromethyl)phenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/856034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant4-(Trifluoromethyl)phenolHCID 67874—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Producttert-Butyl 4-(4-(trifluoromethyl)phenoxy)piperidine-1-carboxylateHCID 2205258644%

Reaction Steps

Tert-butyl 4-hydroxypiperidine-1-carboxylate (2.22 g, 10.0 mmol), 4-hydroxybenzotrifluoride (1.21 g, 7.45 mmol), tri-n-butylphosphine (2.26 g, 11.2 mmol) and 1,1′-(azodicarbonyl)dipiperidine (2.82 g, 11.2 mmol) were dissolved in benzene (20 ml), and the mixture was stirred at room temperature for 2 days. To which water was added, and the mixture was extracted with ethyl acetate. The extract was dried over magnesium sulfate and thereafter filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=5/1) ro afford tert-butyl 4-(4-trifluoromethylphenoxy)piperidine-1-carboxylate (1.13 g, yield 44%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-b82a3f7facff4c2480acc6b04b270c7b
Source noteuspto-grants-2007_08