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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111882Generated: October 27, 2026

Benzaldehyde → N-benzylidene-3,5-dichloroaniline

https://huagongshe.com/reaction/1111882

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 24.6 g. of product, which is recrystallized from pentane to give 18.5 g. of yellow solid, m.p. 52°-53° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04119667
Source datasetuspto-grants-1978_10
ORD IDord-d819304fe79846659f848e04ba34e100
Source noteuspto-grants-1978_10