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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434347Generated: October 30, 2026

4-Cyclohexylbenzenamine → HCID 178419945, compound

https://huagongshe.com/reaction/434347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyclohexylbenzenamineHCID 80764—
ReactantHCID 20493395HCID 20493395—
Solvent1-PentanolHCID 6276—
ProductHCID 178419945HCID 178419945—

Reaction Steps

9.1 g of p-cyclohexylaniline and 11.9 g of 2-n-butylthioimidazolidine hydrobromide in 60 ml of amyl alcohol are refluxed for 6 hours. The solvent is then distilled off in vacuo. The residue is taken up in methylene chloride and successively washed with dilute sodium hydroxide solution and water. The methylene chloride is distilled off and the crude final product is recrystallised from acetonitrile. The resylting 2-(4-cyclohexylphenyl)imino-imidazolidine decomposes at 163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04396617
Source datasetuspto-grants-1983_08
ORD IDord-a7887028543f48a2b3cd5b4abac847b5
Source noteuspto-grants-1983_08