HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 2-(3-Iodophenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 3-Iodobenzyl bromide | HCID 2759361 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3-Iodophenyl)acetonitrile | HCID 2759368 | 90.8% |
Reaction Steps
A mixture of potassium cyanide (4 g) and tetra-n-butylammonium bromide (0.32 g) in water (20 ml) was added to a solution of 3-iodobenzyl bromide (5.92 g) in methylene chloride (20 ml) and the mixture was heated to reflux for 2 hours. The organic phase was separated, washed with water, dried (MgSO4) and evaporated. The residue was purified by column chromatography using methylene chloride as eluent to give 3-iodophenylacetonitrile (4.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05403859 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-0c08671de1f044678774c34865ec61e1 |
| Source note | uspto-grants-1995_04 |