HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2,4,6-Trimethylphenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 2,4,6-Trimethylbenzyl chloride | HCID 74108 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4,6-Trimethylphenylacetonitrile | HCID 520698 | — |
Reaction Steps
66 g of sodium cyanide is refluxed in 100 mL water and 140 mL of ethanol with stirring, until a clear solution is formed. 136 g of 2-chloromethyl-1,3,5-trimethylbenzene is slowly added dropwise to this solution and the mixture is refluxed for 3 hours with stirring. It is diluted with 1 L of water and extracted three times with 200 mL of benzene. The combined organic phases are washed with water and the solvent is distilled off under reduced pressure. The residue is fractionally distilled. Yield: 92 g (72%); bp15: 145° C.-153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06951888B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-cd23e00fb2fd4e78b8755a09f85ebe32 |
| Source note | uspto-grants-2005_10 |