HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → 1-(4-Methylphenyl)-5-cyanoisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | HCID 12851841 | HCID 12851841 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-Methylphenyl)-5-cyanoisoquinoline | HCID 12851842 | 77.4% |
Reaction Steps
A mixture of 22 g of 1-(4-methylphenyl)-5-chloroisoquinoline, 74.4 g of copper cyanide and 420 ml of hexamethylphosphotriamide was heated overnight under reflux. After the reaction, the reaction mixture was poured into a mixture of ethylenediamine, water and benzene, and stirred for 30 minutes. The mixture was then filtered through Celite. The benzene layer as filtrate was washed in water, and dried, followed by distilling off the solvent. The residue was recrystallized from ether to afford 16.4 g of 1-(4-methylphenyl)-5-cyanoisoquinoline as colorless needles having a melting point of 131.8° to 132.4° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04337256 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-b9aea8f511454988b5a7239d2b7982f9 |
| Source note | uspto-grants-1982_06 |