HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylcyanoformamidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylchloroformamidine | HCID 53844528 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylcyanoformamidine | HCID 53839858 | 63.8% |
Reaction Steps
In the manner of Example VII, 7 g of N'-(4-cyano- 3-isopropyl-5-isothiazolyl)-N,N-dimethylchloroformamidine, 3.6 g of anhydrous potassium cyanide, and a catalytic amount of 2,3,11,12-dibenzo-1,4,7,10,13,16-hexaoxacycloocta- 2,11-diene in 200 ml of dry aceto-nitrile were allowed to react for several days. After solvents were removed under reduced pressure, the residue was recrystallized from methylcyclohexane to yield 4.3 g of N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylcyanoformamidine, mp 78°-79°. The ir and nmr spectra were consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04032322 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-4c0630ff68a241df971fa7fe671df2ed |
| Source note | uspto-grants-1977_06 |