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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392483Generated: October 25, 2026

3-(4-Nitrophenyl)prop-2-enal → (E,E)-2-(3,4-Dihydroxybenzylaminocarbonyl)-3-(4-nitrostyryl)acrylonitrile

https://huagongshe.com/reaction/392483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Nitrophenyl)prop-2-enalHCID 15614—
ReactantHCID 178511180HCID 178511180—
Product(E,E)-2-(3,4-Dihydroxybenzylaminocarbonyl)-3-(4-nitrostyryl)acrylonitrileHCID 9947247—

Reaction Steps

The compound was prepared as described in Example 3 by adding 4-nitrocinnamaldehyde (0.009 g, 0.05 mmol) to N-(cyanoacetyl)3,4-dihydroxybenzylamide (Example 2, 0.010 g, 0.05 mmol). After refluxing for 2 h and recrystallization from ethanol a yellow solid was obtained (0.007 g, 39%). The product gave the following analytical data:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800659B2
Source datasetuspto-grants-2004_10
ORD IDord-db425cebb19a4301a6647668f8c97cf4
Source noteuspto-grants-2004_10