HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyclohexylbenzenamine → HCID 178419945, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyclohexylbenzenamine | HCID 80764 | — |
| Reactant | HCID 20493395 | HCID 20493395 | — |
| Solvent | 1-Pentanol | HCID 6276 | — |
| Product | HCID 178419945 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04374143 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-c5f639e2a4a140d5a8362c5280ed714c |
| Source note | uspto-grants-1983_02 |