Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267325Generated: November 1, 2026

4-Chlorobenzaldehyde → HCID 178506597, compound

https://huagongshe.com/reaction/267325

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantHCID 178506596HCID 178506596—
ReactantHCID 178513178HCID 178513178—
ProductHCID 178506597HCID 178506597—

Reaction Steps

In a similar manner the reaction of 1-amino-3-(4-bromobenzylideneamino)guanidine methosulfate with 4-chlorobenzaldehyde gives the methosulfate salt of the subject compound. The reaction of 1-amino-3-(4-cyanobenzylideneamino)guanidine hydroiodide with 4-chlorobenzaldehyde gives 1-(4-chlorobenzylideneamino)-3-(4-cyanobenzylideneamino)guanidine hydroiodide; the reaction of 1-amino-3-(4-chlorobenzylideneamino)guanidine hydrochloride with 4-cyanobenzaldehyde affords the corresponding hydrochloride salt which melts at 297°-298°C. The reaction of 1-amino-3-(3,4-dichlorobenzylideneamino)guanidine hydrobromide and 4-chlorobenzaldehyde gives 1-94-chlorobenzylideneamino)-3-(3,4-dichlorobenzylidenamino)guanidine hydrobromide; the reaction of 1-amino-3-(4-chlorobenzylideneamino)guanidine hydrochloride with 3,4-dichlorobenzaldehyde gives the corresponding hydrochloride salt which melts at 288°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03941825
Source datasetuspto-grants-1976_03
ORD IDord-ba51ea80c5344e45b5c1dc2d35c71b16
Source noteuspto-grants-1976_03