HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(2-Fluoro-4-iodophenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-(Bromomethyl)-2-fluoro-4-iodobenzene | HCID 22240406 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2-Fluoro-4-iodophenyl)acetonitrile | HCID 22240532 | 96.4% |
Reaction Steps
A solution of 2-fluoro-4-iodo-benzyl bromide (Intermediate 1, 2.56 g, 8.15 mmol) in ethanol (55 mL and water (10 mL) was treated with sodium cyanide (2.15 g, 43.86 mmol) and refluxed for 0.5 h. The volatiles were distilled off in vacuo and the residue was diluted with water and extracted with diethyl ether (×2). The combined organic extract was washed with water (×1) and brine (×1), dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford the title compound as a pale yellow solid (2.05 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06855512B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-8c5baf6650944dd3a0aac72d7a35c3d2 |
| Source note | uspto-grants-2005_02 |