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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038482Generated: October 30, 2026

Triethylamine → 4-Cyano-2-methoxyphenyl trifluoromethanesulfonate

https://huagongshe.com/reaction/1038482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant4-Hydroxy-3-methoxybenzonitrileHCID 78135—
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Cyano-2-methoxyphenyl trifluoromethanesulfonateHCID 1665925887%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A mixture of 5-cyano-2-hydroxyanisole (600 mg, mmol) and triethylamine (1.40 mL, 10.0 mmol) was dissolved in anhydrous tetrahydrofuran (20 mL) under argon atomosphere. Trifluoromethanesulfonyl chloride (642 μL, 6.03 mmol) were added thereto at −10° C., and stirred at the same temperature for 1 hour. Ethyl acetate (100 mL) and water (100 mL) were added to the reaction mixture and partitioned. The organic layer was washed with saturated brine (50 mL), dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (979 mg) as a colorless solid. (Yield 87%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551991B2
Source datasetuspto-grants-2013_10
ORD IDord-f2fd0ec01fe946ecabb23c6786ab8b63
Source noteuspto-grants-2013_10