Supported osmates, process for preparation thereof, and a...

Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing

Reexamination Certificate

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C560S060000, C568S860000, C568S633000

Reexamination Certificate

active

06646168

ABSTRACT:

FIELD OF THE INVENTION
The present invention relates to a supported osmate useful as a reusable catalyst in the preparation of vicinal diols. The present invention also relates to a process for the preparation of supported osmates of the formula (S—NR
3
)
2
OsO
4
.nH
2
O wherein S is a support, R is an alkyl group, n is the number of water molecules and use thereof in the preparation of vicinal diols by asymmetric dihydroxylation (AD) of olefins in presence of cinchona alkaloid compounds.
BACKGROUND OF THE INVENTION
Asymmetric dihydroxylation of olefins in the presence of cinchona alkaloid results in products that are important intermediates in the preparation of various drugs and chemicals. For example, the products of cinnamic acid esters are intermediates for taxol side chain, an anticancer drug, diltiazem, calcium antagonist and chloramphenicol, an antibiotic. Proranolol, a &bgr; blocker can also be derived from diols obtained through this method.
There are serious disadvantages in performing the catalytic AD reaction with homogeneous system in the manufacture of vicinal diols due to presence of toxic remnants of osmium in products and high cost of osmium tetraoxide or potassium osmate dihydrate. By employing the heterogeneous catalytic system, the cost naturally comes down due to easy recovery of the catalyst and very insignificant loss of osmium tetraoxide, when compared with homogeneous system. The products thus obtained using heterogeneous catalyst system are benign in the sense that the presence of osmium in minor impurities in the dihydroxylated products is also precluded.
U.S. Pat. Nos. 4,871,855 and 5,260,421 disclose processes for asymmetric dihydroxylation of olefins using osmium tetraoxide and cinchona alkaloids using homogenous catalyst systems. These processes involve cumbersome recovery of the osmium catalyst from the reaction mixture, generation of toxic waste and the potential presence of toxic osmium in the product.
U.S. Pat. Nos. 5,516,929 and 5,260,461 disclose asymmetric dihydroxylation of olefins using osmium tetraoxide and polymer bound cinchona alkaloids in a heterogeneous system. The quantitative recovery of the toxic osmium catalyst, lower enantioselectivity and reduction in activity and enantioselectivity in each recycle experiments are some of the disadvantages associated with this process.
U.S. Pat. No. 5,968,867 discloses asymmetric dihydroxylation of olefins using osmium tetraoxide and silica gel supported bis-cinchona alkaloid derivatives in a heterogeneous system. Quantitative recovery of toxic osmium catalyst is difficult and a reduction in activity and enantioselectivity of the catalyst is observed in each and every recycle experiment.
European Patent 940,170 A2 describes the catalytic asymmetric dihydroxylation of alkenes using a polymer supported osmium catalyst. The drawbacks of this process are that higher amounts of catalyst are required (5 mol %), the reaction time is very long and expensive polymers are used as supports.
OBJECTS OF THE INVENTION
The main object of the invention is to provide a heterogeneous recyclable supported osmate of the general formula (S—NR
3
)
2
OsO
4
.nH
2
O wherein S is a support, R is an alkyl group, n is the number of water molecules and use thereof in the preparation of vicinal diols by asymmetric dihydroxylation (AD) of olefins in presence of cinchona alkaloid compounds.
It is another object of the invention to provide a process for the preparation of a novel heterogeneous recyclable supported osmate of the general formula (S—NR
3
)
2
OsO
4
.nH
2
O wherein S is a support, R is an alkyl group, n is the number of water molecules and use thereof in the preparation of vicinal diols.
It is another object of the invention to provide a environmentally friendly process for the asymmetric dihydroxylation of olefins to obtain vicinal diols using a novel heterogeneous supported osmate of the invention.
It is a further object of the invention to provide a process for the preparation of vicinal diols with good enantioselectivity, activity and yield by the asymmetric dihydroxylation of olefins using a novel osmate catalyst of the invention.
It is yet another object of the invention to provide a process for the preparation of vicinal diols by the asymmetric dihydroxylation of olefins in the presence of cinchona alkaloids and derivatives thereof, which process is simple, economical and results in a product with no traces of toxic osmium therein.
It is a further object of the invention to provide a process for the preparation of vicinal diols by the asymmetric dihydroxylation of olefins in the presence of cinchona alkaloids and derivatives thereof wherein the catalyst is capable of recycle several times without substantial loss of activity or in yield of product.
SUMMARY OF THE INVENTION
These and other objects of the invention are achieved by using the novel supported heterogeneous osmate catalyst of the general formula S—NR
3
)
2
OsO
4
.nH
2
O wherein S is a support, R is an alkyl group, n is the number of water molecules for the asymmetric dihydroxylation of olefins in the presence of cinchona alkaloids to obtain vicinal diols with good yield and selectivity.
The novelty of the invention lies in the supported osmate catalyst and in preparation of vicinal diols in presence of cinchona alkaloids or derivatives employing oxidants.
Accordingly, the present invention provides a supported osmate of the general formula S—NR
3
)
2
OsO
4
.nH
2
O wherein S is a support, R is an alkyl group, n is the number of water molecules.
In one embodiment of the invention, the support is selected from resin and silica.
In another embodiment of the invention, R is selected from methyl, ethyl, propyl, butyl and like alkyl groups.
In a further embodiment of the invention, the osmium content in the catalyst is in the range of 1 to 30%.
In a further embodiment of the invention, the support S as synthesized has charge balancing anions selected from chloride, bromide, iodide, fluoride, hydroxide and acetate.
The invention also relates to a process for the preparation of a novel heterogeneous supported osmate catalyst of the formula S—NR
3
)
2
OsO
4
.nH
2
O wherein S is a support, R is an alkyl group, n is the number of water molecules, said process comprising reacting potassium osmate with a quaternary ammonium species in water.
In one embodiment of the invention, the potassium osmate is of the formula K
2
OsO
4
2H
2
O.
In another embodiment of the invention, the quaternary ammonium species is of the formula S—NR
3
X wherein S is a support, R is alkyl, and X is selected from Cl, Br, I, F, —OH and OAc.
In a further embodiment of the invention, the reaction is carried out at a temperature in the range of 25 to 100° C. for a period in the range of 5-24 hours.
In one embodiment of the invention, the osmium content in the catalyst is in the range of 1 to 30%.
In another embodiment of the invention, the support S is selected from resin and silica.
In a further embodiment of the invention, the support S as synthesized has charge balancing anions selected from chloride, bromide, iodide, fluoride, hydroxide and acetate.
In another embodiment of the invention, R is selected from methyl, ethyl, propyl, butyl and like alkyl groups.
The present invention also provides a process for the preparation of vicinal diols comprising asymmetrically dihydroxylating the corresponding olefin in the presence of a cinchona alkaloid using an oxidant in a solvent selected from the group consisting of water, acetone, acetonitrile, t-butanol and any mixture thereof, at a temperature in the range of −70 to 100° C. for a period in the range of 0.5 to 24 hours, and in the presence of a catalytic amount of a heterogeneous supported osmate catalyst of the general formula S—NR
3
)
2
OsO
4
.nH
2
O wherein S is a support, R is an alkyl group, n is the number of water molecules, and recovering the pure vicinal diol.
In one embodiment of the invention, the osmium content in the catalyst is in the range of 1 to 30%.
In another embodiment of the invention, the support S is selecte

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