HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 2,3-Difluorophenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 1-(Bromomethyl)-2,3-difluoro-benzene | HCID 517984 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,3-Difluorophenylacetonitrile | HCID 518968 | 100.1% |
Reaction Steps
2,3-Difluorobenzyl bromide (5 g, 24.2 mmol) in acetonitrile (20 mL) was treated with 18-crown-6 (638 mg, 2.4 mmol) and potassium cyanide (5 g, 77 mmol). The reaction was heated at reflux for 5.5 hours. The reaction was diluted with diethyl ether (100 mL). The resulting organic solution was washed with 1 N NaOH (3×25 mL), dried over anhydrous MgSO4, filtered, and concentrated to afford 3.71 g of crude 2,3-difluorobenzyl cyanide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07053104B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-b006153201bf4905bdcff29ddbfe4b94 |
| Source note | uspto-grants-2006_05 |