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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267328Generated: October 25, 2026

Hydrazine → HCID 178513179, compound

https://huagongshe.com/reaction/267328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant(4-Chlorobenzyl)hydrazineHCID 3015209—
ReactantHCID 178504058HCID 178504058—
SolventEthanolHCID 702—
ProductHCID 178513179HCID 178513179—

Reaction Steps

The same compound is synthesized by the reaction of equimolar quantities of p-chlorobenzylhydrazine and methyl-3-(4-chlorobenzylidene)thiocarbazimidate hydrochloride (see Example 10) in hot ethanol. It is also prepared by the reaction of equimolar amounts of 1-(p-chlorobenzyl)-S-methylisothiosemicarbazide and hydrazine in warm ethanol, which affords 1-amino-3-(p-chlorobenzylamino)guanidine, followed by treatment of the latter with an equimolar quantity of p-chlorobenzaldehyde in hot isopropanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03941825
Source datasetuspto-grants-1976_03
ORD IDord-d32d94388db0458bbbed5df97ac5fcd2
Source noteuspto-grants-1976_03