HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 10798029, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | 1,3-bis(bromomethyl)-2,4,6-trimethylbenzene | HCID 4386720 | — |
| Product | HCID 10798029 | HCID 10798029 | — |
Reaction Steps
In the above reaction scheme, 1,3-bis(bromomethyl)-2,4,6-trimethylbenzene is reacted with KCN in the presence of a phase transfer catalyst, commonly known as 18-crown-6, (from Aldrich) in acetonitrile. The two-phase system is heated to reflux with vigorous stirring. After two hours, the reaction mixture is cooled, filtered, and evaporated to approximately one-third volume. Distilled water is added, and the mixture is extracted with dichloromethane. The dichloromethane solution is dried over sodium sulfate and filtered, and the solvent evaporated under reduced pressure to obtain 1,3-di(cyanomethyl)-2,4,6-trimethylbenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07390430B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-0131fecb2d8e4e24b4d386ba4c2326ce |
| Source note | uspto-grants-2008_06 |