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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112245Generated: November 2, 2026

Cyanoacetamide → alpha-Cyano-beta-(2-Nitro-4-Fluorophenyl)Acrylamide

https://huagongshe.com/reaction/1112245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetamideHCID 7898—
ReactantPiperidineHCID 8082—
Reactant4-Fluoro-2-nitrobenzaldehydeHCID 76226—
SolventEthanolHCID 702—
Productalpha-Cyano-beta-(2-Nitro-4-Fluorophenyl)AcrylamideHCID 54446537—

Reaction Steps

A mixture of 4-fluoro-2-nitrobenzaldehyde (8.70 g., 51.5 millimoles), 2-cyanoacetamide (4.7 g., 54.4 millimoles), piperidine (0.032 g., 0.37 millimole) and ethanol (80 ml.) is stirred at room temperature for 28 hours. The solid which formed is separated by filtration, washed with ethanol (45 ml.) and dried. Yield = 10 g. (83.5%) of the title acrylamide as light tan crystals M.P. 278°-279° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04120962
Source datasetuspto-grants-1978_10
ORD IDord-c1e98f797e1244c3b2397add21f29b73
Source noteuspto-grants-1978_10