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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844194Generated: October 26, 2026

Trifluoromethanesulfonic anhydride → 3,3,4,4,4-Pentafluorobutyl trifluoromethanesulphonate

https://huagongshe.com/reaction/1844194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant3,3,4,4,4-Pentafluorobutan-1-olHCID 108644—
Product3,3,4,4,4-Pentafluorobutyl trifluoromethanesulphonateHCID 85957581—

Reaction Conditions

Temperature56 °C

Reaction Steps

198.49 g (703.51 mmol) of trifluoromethanesulphonic anhydride were initially charged under argon. The flask was immersed in an oil bath having a temperature of 70° C. and heated to an internal temperature of 56° C. 88.2 ml (738.68 mmol) of 3,3,4,4,4-pentafluorobutanol were added dropwise over a period of 35 min to the reaction mixture. The mixture was stirred at a bath temperature of 70-73° C. and an internal temperature of 69° C. for 2 hours. The reaction mixture was concentrated under reduced pressure and the residue was taken up in 1500 ml of dichloromethane. The mixture was washed once with 300 ml of cold water, once with 300 ml of cold aqueous saturated sodium bicarbonate solution and once with 300 ml of cold water. The organic phase was dried with magnesium sulphate, filtered off and concentrated. This gave 192.86 g (92.6% of theory) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946215B2
Source datasetuspto-grants-2015_02
ORD IDord-b6f42dc766924ab7835334e565fad15b
Source noteuspto-grants-2015_02