Catalytic oxidation of alcohols using manganese oxides

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

Reexamination Certificate

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C568S322000, C568S360000, C568S363000, C568S402000, C568S431000, C568S471000, C568S480000

Reexamination Certificate

active

06486357

ABSTRACT:

BACKGROUND
This invention relates to a method for the catalytic oxidation of alcohols, and in particular, to a method for the selective oxidation of alcohols catalyzed by manganese oxides.
The oxidation of alcohols to carbonyl compounds is of great interest to academia and industry, particularly the fine chemicals industry. A number of catalytic oxidations of alcohols in which oxygen is the secondary oxidant have been reported, using ruthenium, cobalt, copper, palladium, and platinum metal catalysts with additives such as potassium carbonate, sodium bicarbonate, pyridine, molecular sieves, and phenanthroline.
Stoichiometric metal oxidants such as chromium (VI) compounds and active manganese dioxide have also been widely used, particularly for the oxidation of allylic and benzylic oxidations. The reactivity of active manganese oxide is inconsistent, depending on preparation methods, compositions, and structure. Complicated preparation methods are often necessary, and the use of freshly made active manganese oxide is required. Moreover, five to fifty equivalents of these reagents are required to obtain oxidation products, resulting in large amounts of non-reusable, toxic waste. Use of peroxides gives rise to handling hazards.
There accordingly remains a continuing need for cost-effective, efficient, and environmentally friendly methods for the selective oxidation of primary and secondary alcohols to their corresponding aldehydes and ketones.
SUMMARY
A method of oxidizing alcohols comprises reacting an alcohol with oxygen in the presence of an effective amount of a manganese-containing octahedral molecular sieve or a manganese-containing octahedral layer material.
A preferred manganese-containing octahedral molecular sieve has the formula
A
2−y
Mn
8
O
16
.xH
2
O
wherein A is H
+
, Na
+
, or K
+
, y is about 0.5 to about 1.5, and x is 0 to about 20.
Another preferred manganese-containing octahedral molecular sieve has the formula
A
2−y
MnO
2−z
(PO
4
)
z
.xH
2
O
wherein A is H
+
, Na
+
, or K
+
, y is preferably about 0.5 to about 1.5, z is greater than zero to two, and x is 0 to about 20.
Still another preferred manganese octahedral material is a co-synthesized mixture of gamma-manganese oxide and one of the above-described manganese-containing octahedral molecular sieves.


REFERENCES:
patent: 5340562 (1994-08-01), O'Young et al.
patent: 5523509 (1996-06-01), O'Young et al.
patent: 5695618 (1997-12-01), O'Young et al.
patent: 5912388 (1999-06-01), Urch et al.
patent: 6020533 (2000-02-01), Lewis et al.
M. E. Davis, “New Vistas in Zeolite and Molecular Sieve Catalysis”Acc. Chem. Res.1993, 26, 111-115.
I. W. C. E. Arends, et al., “Oxidative Transformations of Organic Compounds Mediated by Redox Molecular Sieves”Angew. Chem. Int. Ed., Engl.1997, 1144-1163.
R. N. DeGuzman, et al., Synthesis and Characterization of Octahedral Molecular Sieves (OMS-2) Having the Hollandite Structure,Chem. Mater.1994, 6, 815-821.
Y.C. Son, et al., “Efficient, Catalytic, Aerobic Oxidation of Alcohols with Octahedral Molecular Sieves”,Angew. Chem. Int. Ed.2001, 40, No. 22.
H. Heineman,Catalysis Reviews Science and Engineering,28(2&3), 185-264 (1986).
R. M. Dessau, “Shape-Selective Reactions of Zeolites. Selective Metal-Catalyst Hydrogenation and Oxidation Using ZSM-5”J. Cataly.,1982, 77. 304.
C-L O'Young, et al., Micropore size distribution of octahedral molecular sieves (OMS),Microporous Materials11, 1997, 1-8.
P. B. Venuto, “Organic catalysis over zeolites; a perspective on reaction paths within micropores,”Microporous Materials 2,1994, 297-411.
C. W. Jones, et al., “Organic-functionalized molecular sieves as shape-selective catalysts”,Chemical Engineer, Nature,1998, 393.
M. Hudlicky,Oxidations in Organic Chemistry,ACS, Washington, DC, 1990, pp. 1-14; 26-37; 114-126; 132-149; 174-182.
C. Song, et al., “Shape-selective alkylation of naphthalene with isopropanol over moredenite catalysts”,Microporous Materials 2,1994, 467-476.
Y. Yoshinaga, et al., “Shape-Selective Hydrogenation and Oxidation over a Platinum-Containing Ultramicroporous Heteropolyoxometallic Compound”,Angew. Chem. Int. Ed. Engl.,1997, 36, 2833.
C. F. Martens, et al., “Shape-Selective Oxidation of Benzylic Alcohols by a Receptor Functionalized with Dicopper(II) Pyrazole Complex”,Am. Chem. Soc.,1994, 116, 5667.
H. B. Friedrich, et al., “The efficient and selective oxidation of alchols with zeolite NaY-supported sodium ruthenate”,J. Mol. Catal. A: Chem.,2000, 160, 401.
J. Luo, et al., “Total oxidationof volatile organic compounds with hydrophobic cryptomelane-type octahedral molecular sieves”,Microporous Material.,2000, 35, 209.

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