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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442199Generated: October 26, 2026

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

https://huagongshe.com/reaction/442199

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., 0.0237 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04044134
Source datasetuspto-grants-1977_08
ORD IDord-25c95626a215461da2793469a09d051f
Source noteuspto-grants-1977_08