HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanide → (3-Methoxy-5-methylphenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanide | HCID 5975 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-(Bromomethyl)-3-methoxy-5-methylbenzene | HCID 585534 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (3-Methoxy-5-methylphenyl)acetonitrile | HCID 22048241 | 70% |
Reaction Steps
To a solution of 3-bromomethyl-5-methylanisole (17 g; 0.008 mol; from step (i) above) in DMSO (25 mL) was added NaCN (8.2 g; 0.16 mol). The mixture, which became very warm upon the addition of the cyanide, was left to cool to room temperature over 1 hour. CH3CN (25 mL) was then added, and the mixture refluxed for 1 hour. The reaction mixture was concentrated, water (200 mL) was added, and the resultant solution was extracted 3 times with ether. The combined organic phase was washed with water, dried (Na2SO4), and concentrated to give 9 g (70%) of the sub-title product as a yellow oil, which was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06838478B2 |
| Source dataset | uspto-grants-2005_01 |
| ORD ID | ord-c2198b3dc0d5438c831245d3c5f63542 |
| Source note | uspto-grants-2005_01 |