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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 904276Erstellt: 25. Oktober 2026

Acetic Acid → Prop-2-enimidic acid--2-(dimethylamino)ethyl 2-methylprop-2-enoate (1/1)

https://huagongshe.com/reaction/904276

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktAcrylamideHCID 6579—
Edukt(Dimethylamino)ethyl methacrylateHCID 17869—
EduktSpan #80 (Sorbitan monooleate)HCID 70693544—
LösungsmittelWaterHCID 962—
ProduktProp-2-enimidic acid--2-(dimethylamino)ethyl 2-methylprop-2-enoate (1/1)HCID 160008—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of 41.9 grams of glacial acetic acid in 350 grams of tap water is added 109.6 grams of dimethylaminoethyl methacrylate (DMAEMA), followed by 148.7 grams of acrylamide (AM). The monomer solution pH is 7.0. It is added slowly to a rapidly stirred solution of 30 grams of sorbitan monooleate (SMO) in 320 grams of Shellflex 131. The resulting emulsion is sparged with nitrogen, warmed to 50° C. and treated with a solution 0.10 grams of bis azoisobutyronitrile (DuPont VAZO) in 2 milliliters of benzene. The polymerization began after a 30 minute induction period. Samples are withdrawn every hour and the residual monomer content determined by gas-liquid chromatography. After 5 hours the DMAEMA had completely disappeared and 20% of the acrylamide was recovered by GLC. This indicates that ≈ 60% of the DMAEMA has been quaternized by the acrylamide. A small portion of the monomer solution was stored at 25° C. for 24 hours. The NMR spectrum showed that 50% of the DMAEMA had been quaternized.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04230839
Quelldatensatzuspto-grants-1980_10
ORD IDord-7227cd480f58417a9ee3981024f89380
Quellennotizuspto-grants-1980_10