Chemistry of hydrocarbon compounds – Aromatic compound synthesis – By condensation of entire molecules or entire hydrocarbyl...
Patent
1988-10-05
1991-03-26
Garvin, Patrick P.
Chemistry of hydrocarbon compounds
Aromatic compound synthesis
By condensation of entire molecules or entire hydrocarbyl...
585466, C07C 268
Patent
active
050031228
ABSTRACT:
The selective isopropylation of a naphthyl compound to diisopropylnaphthalene enhanced in the 2,6-diisopropylnaphthalene isomer is obtained in the presence of an acidic crystalline molecular sieve catalyst having twelve membered oxygen rings. The catalyst pore aperture dimension ranges from 5.5 .ANG. to 7.0 .ANG.. The use of these shape selective catalysts results in a diisopropylnaphthalene stream which is enhanced in .beta. isomers and enhanced in the desired 2,6-diisopropylnaphthalene isomer. A particularly preferred catalyst is synthetic Mordenite. Specific catalyst modifications are also described to improve selectivity to the desired 2,6-diisopropylnaphthalene isomer.
REFERENCES:
patent: 3251897 (1966-05-01), Wise et al.
patent: 3504046 (1970-03-01), Scharf et al.
patent: 3631120 (1971-12-01), Eberly, Jr. et al.
patent: 3637884 (1972-01-01), Vesely et al.
patent: 4026959 (1977-05-01), Kemme et al.
patent: 4064068 (1977-12-01), Hasseltine, Jr.
patent: 4288646 (1981-09-01), Olah
patent: 4415544 (1983-11-01), Kokotailo et al.
patent: 4440871 (1984-04-01), Lok et al.
patent: 4567029 (1986-01-01), Wilson et al.
patent: 4891448 (1990-01-01), Garces et al.
An article entitled "Shape Selective Alkylation of Polynuclear Aromatics with Mordenite-Type Catalysts: A High Yield Synthesis of 4,4-Diisopropylbiphenyl", by Lee et al., Published in Catalysis Letters 2(1989), pp. 243-248.
U.S. PTO Jan. 2, 1990, abstract for U.S. Pat. No. 4,891,465, to Mitsui Petrochemical Industries, Ltd.
Zeolites, Mar. 1990, vol. 10, letter to the editor, "Delocalization of the Acid Function in Molecular Sieves", by Dr. Eric Derouane, 2.
Breck, D. W., Zeolite Molecular Sieves, Structure, Chemistry and Use, a Wiley Inter-Science publication (1974), pp. 59, 64-65.
Meier, W. M. and Olson, D. H.; Atlas of Zeolite Structure Types, 2d Ed., Structure Commission of the International Zeolite Association.
Whyte, Thaddeus (Ed.) et al., Catalytic Materials: Relationship Between Structure and Reactivity, ACS Symposium Series 248 (1983).
Whittingham, M. Stanley, ed., Intercalation Chemistry, pp. 101-146, authored by Eric Derouane.
Studies in Surface Science and Catalysts, 34 p. 143.
Martens, J. A. et al., Zeolites, 1984, 4, Apr., p. 98.
Hildalgo, C. V. et al., Zeolites, 1984, 4, Apr., pp. 175-180.
Philippaerts, J. et al., Analytica Chimica Acta, 195 (1987), pp. 237-246.
Niwa, M. et al., J. Chem. Soc., Faraday Trans. 1, 1984, 80, pp. 3135-3145.
Niwa, M. et al., J. Chem. Soc. Commun., 1982, pp. 819-820.
Peeters, G. et al., Proc. Int. Zeolite Conf., 6th, 1984, pp. 651-659.
Philippaerts, J. et al., Stud. Surf. Sci. Catal., 1986, pp. 319-327.
De Hulsters, P. et al., Stud. Surf. Sci. Catal., 28, 1986, pp. 305-310.
Murakami, Y. Iijima A., and Ward, J. W. (eds.), New Developments in Zeolite Science and Technology, pp. 103-112.
Olah, G. A., J. Am. Chem. Soc., 98, 1976, p. 1839.
Martan, N. et al., Chem. Ind., (London), 1970, p. 434.
Farbevov, M. I. et al., Dokl. Akad. Nauk SSSR, 179(6), 1968, p. 1359.
Frideman, H. M., J. Org. Chem. 34, 1969, p. 3211.
Derouane Eric G.
Fellman Jere D.
Saxton Robert J.
Wentrcek Paul R.
Catalytica Inc.
Garvin Patrick P.
Irzinski E. D.
Wheelock E. Thomas
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