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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099922Generated: November 4, 2026

Water → Cyclohexylbenzene

https://huagongshe.com/reaction/2099922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Cyclohexen-1-oneHCID 13594—
ReactantPhenylboronic AcidHCID 66827—
CatalystAcetylacetonato(1,5-cyclooctadiene)rhodium(I)HCID 10935795—
Solvent1,4-DioxaneHCID 31275—
ProductCyclohexylbenzeneHCID 13229—

Reaction Steps

To a 25-mL three-neck flask were added Rh(acac)(cod) (6.8 mg, 21.8 μmol) and PhB(OH)2 (445 mg, 3.65 mmol), and the atmosphere in the system was substituted with argon. The mixture was added with 3.6 mL of a solution of each ligand (21.8 μmol) in anhydrous dioxane and 2-cyclohexenone (0.073 mL, 0.73 mmol). The mixture was stirred at room temperature for 15 minutes, and added with water (0.18 mL). The reaction mixture was stirred at 100° C. for 3 hours, then added with 9 mL of water, and extracted twice with 9 mL of diethyl ether. The organic layers were combined, washed with 9 mL of saturated sodium chloride solution, and concentrated in an evaporator. The residue was treated by silica gel column chromatography (toluene:ethyl acetate=2:1) to obtain 3-phenylcyclohexane as colorless oil. The resulting optically active 3-phenylcyclohexanone in an amount of 2 mg was dissolved in 1 mL of a mixture of n-heptane and 2-propanol (99:2). This solution was analyzed by HPLC under the following conditions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569730B2
Source datasetuspto-grants-2009_08
ORD IDord-b56e743ac49b4ec9a491057b5dc9ad41
Source noteuspto-grants-2009_08