HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-(4-Chlorobenzyl)-5-cyano-2,2-dimethylcyclopentanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 18323274 | HCID 18323274 | — |
| Product | 5-(4-Chlorobenzyl)-5-cyano-2,2-dimethylcyclopentanone | HCID 11276997 | 72.6% |
Reaction Steps
A 60% mineral oil suspension of sodium hydride (12.7 g, 0.31 mole) in dimethylformamide under nitrogen, is treated with cyano-2,2-dimethylcyclopentanone over a 50 minute period at ice-bath temperatures, then with a solution of 4-chloro-benzyl chloride (50.2 g, 0.31 mole) over a 30 minute period, stirred for 5 hours and quenched with water. The resultant mixture is extracted with ethyl acetate. The extracts are combined, washed with water and concentrated in vacuo to afford a solid residue. The residue is titurated with hexane to afford the title product as white crystals, 59.3 g (72.6% yield), mp 101°-103° C., identified by gas chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06344580B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-6e24075084b24ea6afab7a87b69d1caa |
| Source note | uspto-grants-2002_02 |