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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283156Generated: October 26, 2026

Cyanoacetamide → alpha-Cyano-beta-(2-Nitro-5-Fluorophenyl)Acrylamide

https://huagongshe.com/reaction/1283156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetamideHCID 7898—
ReactantPiperidineHCID 8082—
Reactant5-Fluoro-2-nitrobenzaldehydeHCID 587090—
SolventEthanolHCID 702—
Productalpha-Cyano-beta-(2-Nitro-5-Fluorophenyl)AcrylamideHCID 53864188—

Reaction Steps

A mixture of 3-fluoro-6-nitrobenzaldehyde (10.0 g., 0.0592 mole), 2-cyanoacetamide (5.24 g., 0.0622 mole), piperidine (0.37 g., 4.36 millimole) and ethanol (92 ml.) is heated to reflux on a steam bath for 2 hours. It is then cooled in an ice-bath whereupon the product precipitates and is recovered by filtration, washed with cold ethanol and dried. Yield = 9.1 g. (65%) of crude product. M.P. 162°-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03974161
Source datasetuspto-grants-1976_08
ORD IDord-d62412306aa7472d86ebe729e3e38d78
Source noteuspto-grants-1976_08