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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410311Generated: November 2, 2026

2-Cyclohexen-1-one → 2-Phenylcyclohexanone

https://huagongshe.com/reaction/1410311

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyclohexen-1-oneHCID 13594—
ReactantPhenylboronic AcidHCID 66827—
Product2-PhenylcyclohexanoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921486B2
Source datasetuspto-grants-2014_12
ORD IDord-a251faf949654e0eaaea9d7594335054
Source noteuspto-grants-2014_12