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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181660Generated: November 4, 2026

Oxygen → Adamantanone

https://huagongshe.com/reaction/1181660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantAnisoleHCID 7519—
ReactantAdamantaneHCID 9238—
ReactantN-HydroxyphthalimideHCID 10665—
Reactant1-AdamantanolHCID 64152—
SolventAcetic AcidHCID 176—
ProductAdamantanoneHCID 6415111.3%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 27 g (200 mmol) of adamantane, 3.25 g (20 mmol) of N-hydroxyphthalimide, 0.183 g (0.1 mmol) of V2O5, 240 mL of anisol and 60 mL of acetic acid was stirred for 3 hours at 85° C. and 1 atm (0.101 MPa) in an atmosphere of oxygen. After completion of reaction, the reaction mixture was analyzed by gas chromatography and high performance liquid chromatography, and, as a result, the conversion of adamantane was 13.0%, adamantanol and adamantanone were formed in yield 11.3% (selectivity 86.9%) and yield 0.9% (selectivity 6.9%), respectively. Moreover, in the reaction mixture, 2.12 g of N-hydroxyphthalimide used as a catalyst, 0.68 g of phthalimide, and 0.18 g of phthalic anhydride were contained. The reaction mixture was condensed, 400 mL of hexane was added thereto, and the mixture was stirred for 2 hours at 50° C. After cooling, an insoluble material was filtrated to recover the catalyst and the decomposed product thereof in the form of solid. The filtrate did not contain the catalyst and the decomposed product thereof.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285684B2
Source datasetuspto-grants-2007_10
ORD IDord-33384197acaf4d80a830038cf18a8ab9
Source noteuspto-grants-2007_10