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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1584510Erstellt: 26. Oktober 2026

Sodium Chloride → N-(2,2-Dimethoxyethyl)-2-propenamide

https://huagongshe.com/reaction/1584510

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
EduktAcryloyl chlorideHCID 13140—
EduktSodium HydroxideHCID 14798—
EduktAminoacetaldehyde dimethyl acetalHCID 89728—
Katalysator2,2,6,6-tetramethyl-4-hydroxypiperidine-N-oxideHCID 11607999—
LösungsmittelWaterHCID 962—
ProduktN-(2,2-Dimethoxyethyl)-2-propenamideHCID 989889981,7%

Reaktionsschritte

40 g (1.0 mol) of sodium hydroxide are dissolved in 100 g of water and 200 g of ice in a 1 litre reactor fitted with stirring and cooling means. The sodium hydroxide solution is cooled to 10° C., and 105.1 g (1.0 mol) of aminoacetaldehyde dimethyl acetal and 10 mg of the inhibitor 4-hydroxy-2,2,6,6-tetrarnethylpiperidine 1-oxide are added. 99.5 g (1.1 mol) of acryloyl chloride are slowly added to this solution at 10° C. over the course of 2 hours. The pH drops slowly and is finally set to pH=7. Amine is no longer present according to GC. The reaction mixture is saturated with sodium chloride and extracted three times with 200 ml of tert-butyl methyl ether. The organic phase is dried, filtered and evaporated on a rotary evaporator. The resultant oil is extracted three times with petroleum ether and subsequently re-dried on a rotary evaporator, giving 130 g of acrylamidoacetaldehyde dimethyl acetal (81% of theory) as an oil. The product is 99% pure according to GC. ##STR29##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05932674
Quelldatensatzuspto-grants-1999_08
ORD IDord-9629e37cf3c240cc86c1b4dfe34b6af6
Quellennotizuspto-grants-1999_08