HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Cyano-5-methoxybenzeneacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 28970-91-4 | HCID 12668051 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Cyano-5-methoxybenzeneacetonitrile | HCID 59423525 | — |
Reaction Steps
2-(Bromomethyl)-4-methoxybenzonitrile (36 g, example 235, step 1) was suspended in 200 ml of ethanol, 200 ml of acetonitrile was added followed by KCN (8.3 g) and 150 ml of water. Mixture was stirred and the colorless solution turned to yellow. The reaction was complete after 4 hours of stirring. The volatiles were removed under vacuum, and the residual solid was redissolved in ethyl acetate (200 ml) and washed with water (100 ml) and brine (100 ml). The organics were then dried over sodium sulfate. Ethyl acetate was removed and the residue was recrystallized from ethyl acetate and dichloride methane to provide 17 g of 2-(cyanomethyl)-4-methoxybenzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772180B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-7954d7c1b7084f48809115a2ba5e4db6 |
| Source note | uspto-grants-2010_08 |