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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951381Generated: November 4, 2026

Trifluoromethanesulfonic anhydride → 5-Cyano-2-formylphenyl trifluoromethanesulfonate

https://huagongshe.com/reaction/1951381

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 numberUS08404709B2
Source datasetuspto-grants-2013_03
ORD IDord-685dc25ddbbb47c49bee318c75049295
Source noteuspto-grants-2013_03