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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1112239Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1112239

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., 0.0237 mole) and 2-cyanoacetamide (22.0 g. 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 2 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
PatentnummerUS04120962
Quelldatensatzuspto-grants-1978_10
ORD IDord-5a80ddcc322346fd96bce9216eb8806f
Quellennotizuspto-grants-1978_10