HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Cyclohexen-1-one → 2-Phenylcyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Cyclohexen-1-one | HCID 13594 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Product | 2-Phenylcyclohexanone | HCID 95592 | — |
Reaction Steps
Lastly, to examine the utility of the catalyst on a somewhat larger scale, the reaction of cyclohexenone with phenylboronic acid was performed on a 20 mmol scale and the product 2-phenyl cyclohexanone was isolated in identical yield (83%) to the small-scale reaction (Table 1, entry 5). Thus, the ligands described herein may have practical application in larger scale reactions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08921486B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-a251faf949654e0eaaea9d7594335054 |
| Source note | uspto-grants-2014_12 |