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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211197Generated: November 2, 2026

Allyl bromide → 1,1-Bis(trifluoromethanesulfonyl)-3-butene

https://huagongshe.com/reaction/2211197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantBis[(trifluoromethyl)sulfonyl] methane potassium magnesium chlorideHCID 86749078—
SolventTetrahydrofuranHCID 8028—
Product1,1-Bis(trifluoromethanesulfonyl)-3-buteneHCID 19376110—

Reaction Conditions

Temperature70 °C

Reaction Steps

Next, 4,4-bis[(trifluoromethyl)sulfonyl]-1-butene was prepared by adding 3 ml of allyl bromide to 31.3 millimoles of the bis[(trifluoromethyl)sulfonyl] methane potassium magnesium chloride in 35 ml of THF. The mixture was stirred at 70° C. under reflux for 8 hours. After removal of solvent by distillation under reduced pressure, 50 ml of 3N hydrochloric acid was added to the residue and the aqueous solution was extracted with ethyl ether. The ethyl ether solution was dried with anhydrous MgSO4. The ethyl ether was removed from the solution and the product was distilled at 0.02 torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05463005
Source datasetuspto-grants-1995_10
ORD IDord-f9d445e781a5474593383f9d5006ad80
Source noteuspto-grants-1995_10