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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644166Generated: October 30, 2026

Benzoylhydrazine → N-[(E)-[(E)-3-phenylprop-2-enylidene]amino]benzamide

https://huagongshe.com/reaction/1644166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoylhydrazineHCID 11955—
ReactantCinnamaldehydeHCID 637511—
SolventHexaneHCID 8058—
ProductN-[(E)-[(E)-3-phenylprop-2-enylidene]amino]benzamideHCID 687084690%

Reaction Steps

A mixture of 1a (3.00 g, 22.0 mmol) and trans cinnamic aldehyde (4.35 g, 32.9 mmol, origin: Aldrich) in hexane (100 ml) was stirred at room temperature for 2 h. The reaction mixture was filtered, the residue washed with hexane and dried under vacuum to give 4.95 g (90%) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124578B2
Source datasetuspto-grants-2012_02
ORD IDord-68e97b156d944ea29316e7a2c7a8d981
Source noteuspto-grants-2012_02