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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129354Erstellt: 23. Oktober 2026

Acrylic Acid → N-[3-(Dimethylamino)propyl]-N-[(nonafluorobutyl)sulfonyl]-beta-alanine

https://huagongshe.com/de/reaction/129354

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcrylic AcidHCID 6581—
EduktPhenothiazineHCID 7108—
EduktDiethylene Glycol Monobutyl EtherHCID 8177—
Edukt1-Butanesulfonamide, N-[3-(dimethylamino)propyl]-1,1,2,2,3,3,4,4,4-nonafluoro-HCID 110558—
LösungsmittelWaterHCID 962—
ProduktN-[3-(Dimethylamino)propyl]-N-[(nonafluorobutyl)sulfonyl]-beta-alanineHCID 15251601—

Reaktionsbedingungen

Temperatur125 °C

Reaktionsschritte

An acrylic acid Michael addition reaction was then run according to the general procedure given in U.S. Pat. No. 5,144,069 (Stern et al.). 50 g (0.12 mole) of the purified C4F9SO2N(H)C3H6N(CH3)2, 16.4 g (0.23 mole) of acrylic acid and 0.2 g of phenothiazine (free radical polymerization inhibitor) were added to a 250-mL three-neck flask equipped with an air stirrer and thermometer. The resulting mixture was heated to 125° C. and was allowed to react for 6 hours. After this reaction period, a positive solubility check of the product in water of pH 7 indicated that the Michael addition reaction was essentially complete. While still mixing, a solvent blend of 18 g of diethylene glycol monobutyl ether and 42 g of deionized water was added and the mixture was allowed to cool to room temperature. The water solubility test was run again with the same positive result, showing good conversion to the desired Michael addition product, C4F9SO2N(C2H4COOH)C3H6 (CH3)2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05468353
Quelldatensatzuspto-grants-1995_11
ORD IDord-6db07f2762984316b90d6f5c14a17a70
Quellennotizuspto-grants-1995_11