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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614772Generated: November 1, 2026

Trifluoromethanesulfonic anhydride → (2-Cyano-5-methoxyphenyl)trifluoromethanesulphonate

https://huagongshe.com/reaction/1614772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant2-Hydroxy-4-methoxybenzonitrileHCID 11423680—
SolventPyridineHCID 1049—
Product(2-Cyano-5-methoxyphenyl)trifluoromethanesulphonateHCID 1977185381.1%

Reaction Steps

Trifluoromethanesulphonic anhydride (2.06 g) was added dropwise to a solution of 2-cyano-5-methoxyphenol (1.0 g) in dry pyridine (20 ml) at 0° C. under an atmosphere of argon. Volatile material was removed by evaporation and the residue was dissolved in ethyl acetate (30 ml). The solution was washed with water (60 ml) and saturated sodium chloride solution (30 ml) and dried (MgSO4). The solvent was removed by evaporation and the residue purified by flash chromatography, eluting with ethyl acetate/hexane (1:3 v/v), to give (2-cyano-5-methoxyphenyl)trifluoromethanesulphonate (1.53 g) as an oil; NMR (CDCl3): 3.9(s,3H), 6.95(d,1H), 7.0(d,1H), 7.7(d,1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198439
Source datasetuspto-grants-1993_03
ORD IDord-d1a5297e4c98418ca424bb25d9846b8c
Source noteuspto-grants-1993_03