HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 2-(1-bromonaphthalen-2-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 1-Bromo-2-(bromomethyl)naphthalene | HCID 37828 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(1-bromonaphthalen-2-yl)acetonitrile | HCID 234377 | — |
Reaction Steps
A mixture of 99 parts of 1-bromo-2-(bromomethyl)naphthalene, 103 parts of potassium cyanide and 1 part of benzyl triethylammonium chloride in 150 parts by volume of methylene chloride and 30 parts by volume of water is stirred at room temperature for about 72 hours. The mixture is then diluted with additional quantities of methylene chloride and water, the organic layer separated, dried over calcium sulfate, and concentrated to give α-(1-bromo-2-naphthyl)acetonitrile, as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04217306 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-3bf92dfc906f4dae8a086f25c09d43de |
| Source note | uspto-grants-1980_08 |