Reaktion #9840

ord-580c97f4c2db48c5b59e2f445311d966

Reaktionsgleichung

O=O
oxygene
c1ccc2c(c1)Cc1ccccc1-2
fluorene
CC(=O)On1c(=O)n(OC(C)=O)c(=O)n(OC(C)=O)c1=O
1,3,5-triacetoxy-hexahydro-1,3,5-triazine-2,4,6-trione
→
O=C1C=CC=C2C1=Cc1ccccc12
fluorenon
c1ccc2c(c1)Cc1ccccc1-2
fluorene

Edukte

O=O
oxygene
c1ccc2c(c1)Cc1ccccc1-2
fluorene
CC(=O)On1c(=O)n(OC(C)=O)c(=O)n(OC(C)=O)c1=O
1,3,5-triacetoxy-hexahydro-1,3,5-triazine-2,4,6-trione

Reagenzien

CC(=O)[O-].CC(=O)[O-].[Mn+2]
manganese(II) acetate
CC(=O)[O-].CC(=O)[O-].[Co+2]
cobalt(II) acetate

Lösungsmittel

CC(=O)O
acetic acid

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

A mixture of 1.00 g of fluorene, 0.055 g of 1,3,5-triacetoxy-hexahydro-1,3,5-triazine-2,4,6-trione (3% by mole relative to fluorene), 9.0 g of acetic acid, 0.008 g of cobalt(II) acetate.4H2O and 0.007 g of manganese(II) acetate.4H2O was stirred at 120° C. in an atmosphere of oxygene gas (1 atm=0.1 MPa) for 6 hours. The resulting product in the reaction mixture was analyzed by gas chromatography and was found to yield fluorenon in 93% yield at 99% conversion of fluorene.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091342B2uspto-grants-2006_08