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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159440Generated: October 26, 2026

Dichloromethane → 2-Ethoxyethyl triflate

https://huagongshe.com/reaction/1159440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2,6-LutidineHCID 7937—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant1-EthoxyethanolHCID 10129898—
SolventWaterHCID 962—
Product2-Ethoxyethyl triflateHCID 16050164—

Reaction Conditions

Temperature-5 °C

Reaction Steps

25 g of ethoxyethanol was placed in a round bottom flask provided with a stirrer piece therein, which was connected to a nitrogen bubbler to replace the air in the flask by dry nitrogen. 141 ml of methylene chloride was added and 33 ml of 2,6-lutidine was further added, followed by cooling down to −10 to 0° C., dropping 57 ml of trifluoromethanesulfonic acid anhydride in one hour and continuing agitation under the cooling conditions for one hour. 100 ml of distilled water was added to the reaction solution, and an organic phase was separated, washed with 100 ml of distilled water and dried with anhydrous sodium sulfate, followed by removing the sodium sulfate by filtration and distilling off the solvent under reduced pressure. The resulting residue was distilled under a reduced pressure of 150 Pa at 30° C. to obtain 57 g of a 2-ethoxyethyl triflate fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812155B2
Source datasetuspto-grants-2010_10
ORD IDord-1c58bd53f3f14afa968c57b9eba2f134
Source noteuspto-grants-2010_10