HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408499Generated: October 25, 2026
Allyl bromide → N-Allyl-N-methylnonafluorobutanesulfonamide
https://huagongshe.com/reaction/1408499
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamide | HCID 109968 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Allyl-N-methylnonafluorobutanesulfonamide | HCID 86663271 | 91.1% |
Reaction Steps
A mixture of 313 g (1 mol) N-methylnonafluorobutanesulfonamide (3M Co., U.S. Pat. No. 6,664,354, Savu), 216 g (1 mol) 25% sodium methoxide in methanol (Aldrich), and 100 mL THF (EMD) was stirred at 50° C. for one hour and stripped. The residue was diluted with 600 mL THF and treated with 100 mL (1.15 mol) allyl bromide (Aldrich). The mixture was stirred at 40° C. for about 8 hr and then diluted with water. Extraction with methylene chloride and distillation yielded 321.7 g colorless liquid, by 75-80° C./1.1 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08920679B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-132f713265a1453197029d35e2841a90 |
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| Source note | uspto-grants-2014_12 |
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