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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2163573Erstellt: 26. Oktober 2026

Cyanoacetamide → alpha-Cyano-beta-(2-Nitro-4,5-Dimethoxyphenyl)Acrylamide

https://huagongshe.com/reaction/2163573

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanoacetamideHCID 7898—
EduktPiperidineHCID 8082—
Edukt6-NitroveratraldehydeHCID 88505—
LösungsmittelMethanolHCID 887—
Produktalpha-Cyano-beta-(2-Nitro-4,5-Dimethoxyphenyl)AcrylamideHCID 4145653—

Reaktionsschritte

Piperidine (2.1 g., 0.0237mole) and 2-cyanoacetamide (22.0g., 0.263 mole) are added to a slurry of 6-nitroveratraldehyde (50.0 g., 0.237 mole) in methanol (500 ml.). The mixture is heated to reflux for two hours, and then cooled in an ice bath and filtered. The bright yellow filter cake is washed with cold isopropanol (300 ml.) and then air dried. Yield = 60.1 g. (93%); m.p. 265°-266° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04134981
Quelldatensatzuspto-grants-1979_01
ORD IDord-2e88bbac5f924a2cb8269c8b139714cc
Quellennotizuspto-grants-1979_01