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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439147Generated: October 30, 2026

p-Toluenesulfonic acid → Benzonitrile, 4-[[(4-pentylphenyl)methylene]amino]-

https://huagongshe.com/reaction/1439147

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-AminobenzonitrileHCID 13396—
ReactantBenzaldehyde, 4-pentyl-HCID 23290—
SolventBenzeneHCID 241—
ProductBenzonitrile, 4-[[(4-pentylphenyl)methylene]amino]-HCID 170810—

Reaction Steps

A mixture of 5.9 g. of p-aminobenzonitrile and 8.8 g. of p-n-pentylbenzaldehyde in 100 ml. of benzene is treated with 150 mg. of p-toluenesulfonic acid and reacted as described in Example 1. After evaporation, there remain 13.9 g. of a yellow oil which crystallizes with cooling. Purification is carried out by several recrystallizations from isopropanol as described in Example 1. The p-[(p-n-pentylbenzyliden)amino]benzonitrile which is obtained has a melting point of 45.6°-46.4° C. and a clearing point of 75.0° C. UV (ethanol): ε279 = 24400 (shoulder at 314 nm). The nuclear magnetic resonance, mass spectrum, infrared and microanalysis data confirm the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04058477
Source datasetuspto-grants-1977_11
ORD IDord-a51e00c59c41458cae0cf0ea0091a311
Source noteuspto-grants-1977_11