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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Bis[(trifluoromethyl)sulfonyl] methane potassium magnesium chloride | HCID 86749078 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,1-Bis(trifluoromethanesulfonyl)-3-butene | HCID 19376110 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05463005 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-f9d445e781a5474593383f9d5006ad80 |
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| Source note | uspto-grants-1995_10 |
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