HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 4-(Pyridin-4-YL)butanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 4-(3-Chloropropyl)pyridine | HCID 205442 | — |
| Catalyst | Dibenzo-18-crown-6 | HCID 26541 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(Pyridin-4-YL)butanenitrile | HCID 13557531 | 84.5% |
Reaction Steps
To the product of Example 21 (6.7 g, 42.9 mmol) in 300 mL of acetonitrile (CH3CN), was added potassium cyanide (KCN, 11.2 g, 171.7 mmol) and dibenzo-18-crown-6 (1.0 g, 2.8 mmol). After the reaction had been refluxed for 18 hours, it was cooled to room temperature, and stripped of all solvent under reduced pressure. The residue was partitioned between 100 mL each of water and CH2Cl2 and the aqueous phase was washed with 3×100 mL of CH2Cl2. The combined organic phase was dried (Na2SO4), filtered, and stripped of solvent to yield 6.7 g of crude product. This material was purified by HPLC on silica gel to yield 5.3 g of the title material as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05504077 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-34028e911a1d4e688f05758eee4b26e0 |
| Source note | uspto-grants-1996_04 |