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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41633Generated: October 25, 2026

Phenol → Trifluoroacetic acid

https://huagongshe.com/reaction/41633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
Reactant4-[2-(Toluene-4-sulfonyloxymethyl)furan-3-yl]piperidine-1-carboxylic acid t-butyl esterHCID 58442832—
SolventAcetonitrileHCID 6342—
ProductTrifluoroacetic acidHCID 642288%
Product4-(2-Phenoxymethylfuran-3-yl)piperidineHCID 53390869—

Reaction Conditions

Temperature50 °C

Reaction Steps

4-[2-(Toluene-4-sulfonyloxymethyl)furan-3-yl]piperidine-1-carboxylic acid t-butyl ester (65 mg, 0.15 mmol, 1.0 eq.) was dissolved in MeCN (770 μL) and added to a mixture of potassium carbonate (32 mg, 230 mmol, 1.6 eq.) and phenol (21.1 mg, 224 μmol, 1.5 eq.). The resulting mixture was shaken at 50° C. overnight. The mixture was then cooled and the solids removed. The supernatant was combined with TFA (12 μL, 160 mmol, 1.0 eq.) and the resulting mixture was shaken overnight at room temperature. The solution was concentrated using an evaporator, then dissolved in 1:1 AcOH:H2O (5.0 mL) then an additional 2.0 ml AcOH, filtered, and purified by preparative HPLC to yield the title compound as a TFA salt (1.4 mg, 88% purity). MS m/z: [M+H]+ calcd for C16H19NO2, 258.14. found 258.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530663B2
Source datasetuspto-grants-2013_09
ORD IDord-21939524e57f442fb56cf51e501b04c2
Source noteuspto-grants-2013_09