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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049532Generated: October 26, 2026

Benzaldehyde → N-benzylidene-3,5-dichloroaniline

https://huagongshe.com/reaction/2049532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantMethaneHCID 297—
Reactant3,5-DichloroanilineHCID 12281—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventTolueneHCID 1140—
ProductN-benzylidene-3,5-dichloroanilineHCID 962139—

Reaction Steps

To a reaction flask, equipped with a Dean-Stark trap, is added 3,5-dichloroaniline (16.2 g., 0.10 mole), benzaldehyde (10.6 g., 0.10 mole), p-toluenesulfonic acid monohydrate (0.2 g.), and toluene (100 ml.). The reaction mixture is then warmed to reflux and the water (1.65 ml.) collected by azeotroping. The cooled reaction mixture is treated with charcoal and the filtrate reduced in vacuo to give an amber oil that crystallizes on standing to give N-benzylidene-3,5-dichloroaniline which is recrystallized from pentane. m.p. 52°-53° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198349
Source datasetuspto-grants-1980_04
ORD IDord-6e25c6e8d5904ed39b948eae8e3706a8
Source noteuspto-grants-1980_04