Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2000-11-08
2002-01-08
Higel, Floyd D. (Department: 1626)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
active
06337407
ABSTRACT:
DESCRIPTION
Pyrethroids are an important class of insecticides whose activity is based on a strong action on the sodium channels in the nerve membranes of insects.
WO-A 99/32426 describes derivatives of 2,2-dimethyl-3-(2-fluorovinyl)cyclopropanecarboxylic acid as highly active pyrethroids. The preparation of this acid is carried out by multistep reductive transformation of 2,2-dimethyl-3-(2-fluoro-3-hydroxy-3-oxo-1-propenyl)cyclopropane-carboxylic acid esters.
It was an object of the present invention to provide novel advantageous synthesis routes for the acid and thus for the pyrethroids mentioned.
Surprisingly, it has now been found that 2,2-dimethyl-3-(2-fluorovinyl)cyclopropanecarboxylic acid can be prepared in simple manner in high purity and good yields by halofluorination of 4,7,7-trimethyl-3-oxabicylo[4.1.0]hept-4-en-2-one to give the novel 5-halo-4-fluoro-4,7,7-trimethyl-3-oxabicyclo[4.1.0]heptan-2-ones, followed by reductive elimination.
Halofluorination of enollactones is known in principle (see M. Brand and S. Rozen, J. of Fluorine Chem. (1982), 20, 419 or Houben-Weyl, Methoden der organischen Chemie [Methods of organic chemistry], Vol. E 10).
However, halofluorination is limited to only those substrates which are stable under halofluorination conditions. Furthermore, it is known that cyclopropane or its derivatives react with HF or even with HF/Py even at room temperature with ring-opening and formation of fluoropropanes or cyclobutane derivatives (see, for example, J. Org. Chem. (1979), 44, 3873 or Tet. Lett. (1987), 28, 6313).
Bicyclic enollactones comprising three-membered rings are highly sensitive to acids, bases and oxidizing agents and usually react with opening of the lactone or cyclopropane ring. Because of this, it is surprising that the chloro-, bromo- or iodofluorination of enollactones gives chlorofluoro, bromofluoro or iodofluoro compounds in good yields and high purities.
The invention provides halogenated lactones of the formula (I),
in which Hal is Cl, Br or I.
The compounds of the formula (I) embrace all possible stereoisomers.
Compounds of the formula (I) are highly suitable for use as intermediates in the preparation of pyrethroids, as described in WO-A 99/32426.
The compounds of the formula (I) are prepared by reacting an enollactone (II) with a halofluorinating agent (“HalF”)
in which Hal is Cl, Br or I.
This process also forms part of the subject matter of the invention.
The term halofluorinating agent is to be understood as meaning reagents or combinations thereof capable of transferring positive halogen atoms and fluoride anions to organic compounds.
The reaction can be carried out with ClF, BrF (see, for example, M. Brand and S. Rozen, J. of Fluorine Chem. (1982), 20, 419) or preferably with an equivalent, comprising a compound which contains one or more positive halogen atoms (Hal
+
), and also hydrofluoric acid or salts thereof (see, for example, F. Camps et al., J. Org. Chem. (1989), 54, 4294).
Preferred Hal
+
sources are N-chloroacetamide, hexachioromelamine, N-bromoacetamide, N-chlorosuccinimide (NCIS), N-bromosuccinimide (NBS), N-iodosuccinimide, 1-bromo-3,5,5-trimethylhydantoin, N,N-dibromo-5,5-dimethylhydantoin (DBH), and other halogenating agents are also possible. It is also possible to use a mixture of two or more halogen compounds. Particularly preferred halogenating agents are NBS and DBH, and very particular preference is given to DBH.
The fluorides used are, in general, fluorides of the formula (III):
KAT H
n
F
n+1
(III)
in which KAT denotes a stoichiometric equivalent of an alkaline earth metal ion, an alkali metal ion, a tetraalkylammonium ion, a tetraalkylphosphonium ion, a tetraarylphosphonium ion or a tetrakis(dialkylamino)phosphonium ion, where alkyl is an alkyl group with preferably 1 to 6 carbon atoms, aryl is an aryl group with 6 to 12 carbon atoms and n is 0, 1, 2, 3, 4 or 5.
Without the lists being known to be complete, the following fluorides may be mentioned:
Potassium hydrogen difluoride, potassium tetrahydrogen pentafluoride, tetramethylammonium fluoride, tetramethylammonium hydrogen difluoride, tetramethylammonium dihydrogen trifluoride, tetraethylammonium hydrogen difluoride, tetrabutylammonium hydrogen difluoride, tetrabutylammonium dihydrogen trifluoride, benzyltrimethylammonium hydrogen difluoride, tetraphenylphosphonium hydrogen difluoride, tetrakis(diethylamino)phosphonium hydrogen difluoride, HF, HF/pyridine complex, Et
3
N×3HF, Bu
3
N×3HF. It is also possible to use a mixture of two or more fluorides. It is furthermore possible to use systems of fluorine-containing compounds and water, for example SiF
4
/H
2
O, SbF
3
/H
2
O, AlF
3
/H
2
O. It is furthermore possible to use [ClF] from Cl
2
and F
2
or [BrF] from Br
2
and F
2
(see, for example, M. Brand and S. Rozen, J. of Fluorine Chem. (1982), 20, 419).
The process can be carried out in the presence or absence of a solvent. If solvents are used, both polar and nonpolar solvents are suitable. Suitable solvents are, for example: hexane, cyclohexane, dioxane, diethyl ether, diisopropyl ether, toluene, dichloromethane, dichloroethane and polyethers.
The reaction temperature is usually between −30 and +30° C., preferably between −15 and +20° C., and depends, inter alia, on the type of the halofluorinating agent, in the manner known to the person skilled in the art.
The fluorides are generally employed in amounts of from 0.2 to 2, in particular from 0.25 to 1.5, preferably from 0.4 to 1 mol, based on 1 mol of enollactone. The amount of fluoride depends on the number of fluoride atoms in the molecule. Thus, the use of HF requires twice the amount, compared to tetrabutylammonium hydrogen difluoride. It has to be taken into account that there may be cases where an excess of fluoride may lead to undesirable side reactions. In these cases, it is recommended to use a substoichiometric amount of fluoride.
The halogenating agent is generally employed in an amount of from .5 to 2 mol, preferably from 0.4 to 1 mol, based on 1 mol of enollactone. The amount of halogenating agent depends on the number of halogen atoms in the molecule. Thus, the use of N-bromosuccinimide requires twice the amount, compared to dibromohydantoin.
The enollactone of the formula (II) embraces all possible stereoisomeric forms. It is known and can be synthesized by methods known from the literature (see, for example, D. Bakshi et al., Tetrahedron (1989), 45, 767).
The halofluorination of enollactones of the formula (II) gives an isomer mixture of a plurality of stereo isomers; in the case of the bromofluorination of (1R,6S)-4,7,7-trimethyl-3-oxabicyclo[4.1.1]hept-4-en-2-one, for example, an isomer mixture of mainly three stereoisomers is formed:
However, in a simple manner, known to the person skilled in the art, it is possible to influence the isomer ratios by reaction conditions (time, temperature etc.) (see Table 1 in the examples). Isomer A can be isolated in pure form by crystallization from alcohol. The other isomers can be isolated by chromatography, for example by medium pressure liquid chromatography (MPLC) using hexane/ethyl acetate mixtures.
The compounds of the formula (I) can be reacted further with a reducing agent to give cis-cyclopropanecarboxylic acids of the formula (IV):
This process and a process for preparing cyclopropanecarboxylic acids of the formula (IV) by successive halofluorination and reduction of the enollactone (II) also form part of the subject matter of the invention.
Suitable reducing agents are all customary reducing agents, such as Mg, Fe, Zn, Sn, Al, Bu
3
SnH, LiAIH
4
(see, for example, J. Am. Chem. Soc., 121, 4155, 1990). The cyclopropanecarboxylic acid of the formula (IV) can be formed as a mixture of two geometrical isomers.
The acid of the formula (IV) or a functional derivative of the acid can be converted with a compound of the formula (V),
R—X (V)
in which X is a leaving group, preferably OH, Cl, Br, I, OTosyl (
Babin Didier
Demoute Jean Pierre
Hömberger Günter
Pazenok Sergej
Aventis CropScience GmbH
Frommer & Lawrence & Haug LLP
Higel Floyd D.
Shameem Golam M. M.
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