HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → 2-(4-Bromo-3-fluorophenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-Bromo-4-(bromomethyl)-2-fluorobenzene | HCID 11666176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Bromo-3-fluorophenyl)acetonitrile | HCID 11600953 | 155.7% |
Reaction Steps
A solution of 4-bromo-3-fluorobenzyl bromide (12.2 g, 0.03 moles) in ethanol (100 ml) is added with NaCN (2 g, 0.04 moles) and refluxed for 2 hours. The mixture is concentrated under vacuum; the resulting residue is taken up with water, then extracted with ethyl acetate. The organic phase is washed with brine, dried over sodium sulfate and concentrated under vacuum to give a dark oil (10 g), which is subjected to chromatography on a silica gel column (150 g), eluting with hexane:ethyl ether 7:3, to afford the product in the solid form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662995B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-15074058e8c64594871f4e432909e2e3 |
| Source note | uspto-grants-2010_02 |