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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1408499Erstellt: 26. Oktober 2026

Allyl bromide → N-Allyl-N-methylnonafluorobutanesulfonamide

https://huagongshe.com/reaction/1408499

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
Edukt1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamideHCID 109968—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-Allyl-N-methylnonafluorobutanesulfonamideHCID 8666327191,1%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08920679B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-132f713265a1453197029d35e2841a90
Quellennotizuspto-grants-2014_12