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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951373Generated: November 2, 2026

Trifluoromethanesulfonic anhydride → 4-Cyano-2-methoxyphenyl trifluoromethanesulfonate

https://huagongshe.com/reaction/1951373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant4-Hydroxy-3-methoxybenzonitrileHCID 78135—
SolventPyridineHCID 1049—
Product4-Cyano-2-methoxyphenyl trifluoromethanesulfonateHCID 16659258—

Reaction Steps

24 ml (141 mmol) of trifluoromethanesulfonic anhydride are slowly added dropwise to a solution of 20 g (134 mmol) of 4-hydroxy-3-methoxybenzonitrile in pyridine (80 ml), keeping the reaction temperature below 25° C. with the aid of an ice bath. The suspension is then stirred at RT for 1 h. Ice-water (400 ml) is added, and the suspension is stirred further until room temperature is reached. It is then filtered, the solid is dissolved in ethyl acetate, and the solution is washed with saturated sodium chloride solution. The organic phase is dried over magnesium sulfate and concentrated. 37.13 g (92% of theory) of the title compound are obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404709B2
Source datasetuspto-grants-2013_03
ORD IDord-8e66974c68ff43a1a22f476b38dfcd96
Source noteuspto-grants-2013_03