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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163573Generated: October 27, 2026

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

https://huagongshe.com/reaction/2163573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetamideHCID 7898—
ReactantPiperidineHCID 8082—
Reactant6-NitroveratraldehydeHCID 88505—
SolventMethanolHCID 887—
Productalpha-Cyano-beta-(2-Nitro-4,5-Dimethoxyphenyl)AcrylamideHCID 4145653—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04134981
Source datasetuspto-grants-1979_01
ORD IDord-2e88bbac5f924a2cb8269c8b139714cc
Source noteuspto-grants-1979_01