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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622865Generated: November 1, 2026

Pyridine → HCID 86636040, compound

https://huagongshe.com/reaction/1622865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-CumylphenolHCID 11742—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
SolventAcetonitrileHCID 6342—
ProductHCID 86636040HCID 86636040—

Reaction Steps

Trifluoromethanesulfonic anhydride (1.99 mL) was added dropwise to a solution of 4-(2-phenylpropan-2-yl)phenol (1.68 g) and pyridine (1.277 mL) in MeCN (10 mL) at 0° C. The mixture was stirred at room temperature for 2 days. The mixture was quenched with 0.1 N HCl aq. at 0° C. and extracted with EtOAc. The organic layer was separated, washed with water and brine, dried over anhydrous magnesium sulfate, filtered through silica-Celite pad (eluted with EtOAc) and concentrated in vacuo to give 4-(2-phenylpropan-2-yl)phenyl trifluoromethanesulfonate (2.65 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778934B2
Source datasetuspto-grants-2014_07
ORD IDord-3f9276b8224645fd9859a3ddf2b5e2ab
Source noteuspto-grants-2014_07