HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 3-Cyclohexyl-3-oxopropanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Methyl cyclohexanecarboxylate | HCID 20748 | — |
| Reactant | HCID 178418261 | HCID 178418261 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Cyclohexyl-3-oxopropanenitrile | HCID 11309597 | — |
Reaction Steps
A solution of 0.53 mL (10 mmol) of MeCN in 5 ml of THF was cooled in −78° C. bath and 12 mL of 1M LiN(TMS)2 was added. After 5 min, 0.75 mL (5.2 mmol) of methyl cyclohexane carboxylate was added. The cold bath was removed after 1 hr and stirring was continued for another 1 hr. The reaction was acidified with 1.2 N HCl and extracted with ether. The ether layer was washed with brine, dried and concentrated. The residue was chromatographed using a gradient of 10-50% EtOAc-hexane to furnish the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07390835B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-0fd634d9f9dd4fc187e65e5ee4606e2b |
| Source note | uspto-grants-2008_06 |