Preparation of fluorinated dicarbonyls

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

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549291, 560 51, 560122, 560125, 560174, 560178, 568316, 568348, 568393, C07D30758, C07C 6730, C07C 4565

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active

060205024

DESCRIPTION:

BRIEF SUMMARY
FIELD OF THE INVENTION

The present invention relates to the preparation of dicarbonyls, in particular dicarbonyl compounds which are 2-fluoro- and 2,2-difluoro-1,3-diketones and -ketoesters.


BACKGROUND OF THE INVENTION

The use of elemental fluorine for the site specific fluorination of aliphatic compounds is rarely satisfactory due to the high reactivity of the element which leads to unspecific multiple substitution, carbon-carbon bond cleavage and oxidation. Because of the growing importance of fluorinated organic compounds in applications such as in biochemical systems, (Ref 1: R Filler, Y Kobayashi (editors); Biomedical Aspects of Fluorine Chemistry; Elsevier Biomedicinal Press, New York, 1982), (Ref 2: J T Welch; Tetrahedron, 1987, 43, (14), 3123) in recent years considerable effort has gone into finding ways of introducing fluorine into specific sites within molecules to provide building blocks for the preparation of biologically active compounds which have more complex structures. In this context, the replacement of the 2 hydrogen in 1,3-diketones and 1,3-ketoesters is just one transformation that has aroused much interest since the mono- and/or di-fluorinated products can be useful intermediates in the preparation of bio-active molecules. This transformation has been carried out either by treating the 1,3-diketone or 1,3-ketoester or their metal enolates with one of several "electrophilic fluorinating agents" that have been developed recently. For example, 1,3-diketones and 1,3-ketoesters have been treated with acetyl hypofluorite (Ref 3: S Rozen and O Lerman; J. Org. Chem., 1983, 48, 724), N-fluoro-pyridinium salts with or without a Lewis Acid catalyst (Ref 4: T Umemoto et al; J Amer. Chem. Soc., 1990, 112, 8563), xenon difluoride (Ref 5: B Zajc and M Zupan; J Chem Soc., Chem Commun, 1980, 759), lamellar C.sub.19 XeF.sub.6 (Ref 6: H B Kagan, S S Yemul and R Setton; Tetrahedron Letts., 1980, 21, 277), and N-fluorobis[(perfluoroalkyl)sulphonyl]imides (Ref 7: G Resnati and D D Desmarteau; J Org. Chem., 1992, 57, 4281) (Ref 8: Z Xu, D D Desmarteau and Y Gotoh; J Fluorine Chem., 1992, 58, 71), (Ref 9: G Resnatti and D D Desmarteau; J. Org. Chem., 1991 56, 4925), (Ref 10 Z Xu, D D Desmarteau and Y Gotoh; J Chem Soc; Chem. Commun; 1991, 179) and their metal enolates have been treated with acetyl hypofluorite (Ref 3), N-fluoro-pyridinium salts (Ref 4).
Thus, although the treatment of 1,3-diketones and 1,3-ketoesters with electrophilic fluorinating agents can sometimes give high yields of the required mono- or di-fluorinated products, some of these reagents decompose fairly quickly, and the compounds from which they are made are often expensive or difficult to obtain.


SUMMARY OF THE INVENTION

According to the present invention there is provided a method for the production of 1,3-dicarbonyls of formula (1), (2), (3) or (4) as follows: ##STR1## which comprises converting the corresponding compound of formula (5), (6), (7) or (8) as follows: ##STR2## into compounds of formula (1), (2), (3) or (4) by reaction with elemental fluorine, wherein R.sub.1 is selected from alkyl, substituted alkyl, cycloalkyl, aryl, substituted aryl and acetoxy, R.sub.2 is selected from hydrogen, halogen, nitro, cyano, alkyl, cycoloalkyl, acetoxy and aryl substituted alkyl, acetoxy, aryl and substituted aryl, and R.sub.3 is selected from alkyl, substituted alkyl, oxyalkyl and substituted oxyalkyl, R.sub.4 and R.sub.5 are hydrogen or alkyl n is an integer in the inclusive range 1 to 8 and the structures represented by formula (2), (3), (4), (6), (7) and (8) are cyclic, the process being carried out by passing fluorine gas into a solution of the appropriate compound of formula (5), (6), (7) or (8) in a substantially inert solvent comprising an acid such as formic acid of a mixture of neutral and acid solvents.
Where any one of the groups R.sub.1, R.sub.2 and R.sub.3 is an alkyl, cycloalkyl or aryl group the group may include one or more optional substituents or hetero atoms.
Where R.sub.2 in formula (5) is hydrogen, R.sub.2 in fo

REFERENCES:
patent: 5569778 (1996-10-01), Umemoto et al.

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