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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170950Generated: October 30, 2026

Trifluoromethanesulfonic anhydride → 5-Cyano-2-formylphenyl trifluoromethanesulfonate

https://huagongshe.com/reaction/2170950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Formyl-3-hydroxybenzonitrileHCID 12813648—
SolventDichloromethaneHCID 6344—
Product5-Cyano-2-formylphenyl trifluoromethanesulfonateHCID 59349638—

Reaction Steps

2.4 ml (14.27 mmol) of trifluoromethanesulfonic anhydride are added dropwise to a solution of 2 g (13.59 mmol) of 4-formyl-3-hydroxybenzonitrile and 2.5 ml (14.27 mmol) of N,N-diisopropylethylamine in 37 ml of anhydrous dichloromethane at 0° C. under an argon atmosphere. The reaction mixture is stirred at RT for 1 h, then diluted with 70 ml of dichloromethane and washed successively with 1 M hydrochloric acid, saturated sodium bicarbonate solution and saturated sodium chloride solution. The organic solution is dried over magnesium sulfate and concentrated. The residue is purified by column chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 7:1). 2.36 g (62% of theory) of the title compound are obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051316B2
Source datasetuspto-grants-2015_06
ORD IDord-0e219f00444a4ff183595d10e04e045d
Source noteuspto-grants-2015_06