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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382452Generated: October 29, 2026

Perfluoro-1-butanesulfonyl fluoride → HCID 86755183, compound

https://huagongshe.com/reaction/382452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerfluoro-1-butanesulfonyl fluorideHCID 67814—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 86755181HCID 86755181—
SolventTolueneHCID 1140—
ProductHCID 86755183HCID 86755183—

Reaction Conditions

Temperature-15 °C

Reaction Steps

Under a nitrogen atmosphere, (R)-8-(2-(2-(2-(trifluoromethoxy(tetrafluoroethoxy) tetrafluoroethoxy)-2,2-difluoroethoxy)-7-hydroxyoct-1-ene (60 g, 0.103 mol) and dry toluene (120 mL) were added to an oven-dried flask with stirring. The resulting solution was cooled to −15° C., perfluorobutanesulfonyl fluoride (58.9 g, 0.185 mol) was added, and the resulting reaction mixture was stirred for 5 minutes. 1,8-Diazabicyclo[5.4.0]undec-7-ene (28.7 g, 0.189 mol) was then added at a rate so as not to exceed a temperature of 5° C. for the reaction mixture. The reaction mixture was stirred for 1 hour at ambient temperature and was quenched by the addition of toluene (120 mL) and water (60 mL). The resulting organic phase was separated from the resulting aqueous phase, and the aqueous phase was washed with toluene. The combined organic extracts were washed with 120 mL of 7 volume % HCl. The combined extracts were concentrated under reduced pressure (25 torr), and the resulting crude product was distilled (b.p. 58-65° C. at 0.01 torr) to give 33.8 g of (S)-8-(2-(2-(2-(trifluoromethoxy(tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)-7-fluorooct-1-ene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06309561B1
Source datasetuspto-grants-2001_10
ORD IDord-3fea71b6b7fd4a9881c16795db439351
Source noteuspto-grants-2001_10