HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → Hydrochloric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Dibenzo-18-crown-6 | HCID 26541 | — |
| Reactant | 5-(5-Chloropentyl)imidazo[1,5-a]pyridine | HCID 20446676 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | 5-(5-Cyanopentyl)-imidazo[1,5-a]pyridine hydrochloride | HCID 20446665 | — |
Reaction Steps
A solution of 37 g of 5-(5-chloropentyl)-imidazo[1,5-a]pyridine, 21.7 g of potassium cyanide and 3 g of dibenzo-18-crown-6 in acetonitrile is heated under reflux for 20 hours. The acetonitrile is evaporated under reduced pressure, the residue is partitioned between water and methylene chloride, and the methylene chloride extract is evaporated to dryness. Treatment of a solution of the residue in ether with ethanolic hydrochloric acid yields 5-(5-cyanopentyl)-imidazo[1,5-a]pyridine hydrochloride melting at 178°-80°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04470986 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-7bbda157222d44e89a43344261bb1458 |
| Source note | uspto-grants-1984_09 |