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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604312Generated: November 1, 2026

Benzaldehyde → Benzaldehyde 4-(4-chloro-alpha-cyanobenzyl)-3,5-dichlorophenyl hydrazone

https://huagongshe.com/reaction/1604312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant4-(4-Chloro-alpha-cyanobenzyl)-3,5-dichlorophenyl hydrazineHCID 22008537—
SolventEthyl AcetateHCID 8857—
ProductBenzaldehyde 4-(4-chloro-alpha-cyanobenzyl)-3,5-dichlorophenyl hydrazoneHCID 86754869—

Reaction Steps

In 30 ml of acetic acid ethyl ester was dissolved 3.26 g of 4-(4-chloro-α-cyanobenzyl)-3,5-dichlorophenyl hydrazine. To the solution was added equimolar benzaldehyde and three times as much mol. of anhydrous magnesium sulfate, then the reaction was allowed to proceed for one hour at room temperature. After completion of the reaction, insolubles were removed, and the solution was concentrated, which was recrystallized from acetonitrile to afford 3.3 g of the titled compound as colorless crystals, m.p. 162-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994355
Source datasetuspto-grants-1999_11
ORD IDord-9d8c3e46758e4b79a0902c3818dd0ac0
Source noteuspto-grants-1999_11