Production of lactones from diols

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

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549273, 549295, 549299, 549323, C07D30732

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active

051069954

ABSTRACT:
A method for converting 1,4 and 1,5 aliphatic saturated diols to lactones is disclosed wherein the diol is reacted with a chemical oxidizing agent and a ruthenium containing catalyst at temperatures substantially less than 200.degree. C. The reaction proceeds quickly and produces high yields of the desired product.

REFERENCES:
patent: 4465847 (1984-08-01), Shvo
H. Mercker, et al., Ulmanns Encyclopedia of the Chemical Industry, "Batgrolactone," A4, pp. 495-498 (1957).
S. Murahashi, et al., J. Org. Chem., "Ruthenium-Catalyzed Oxidations of Alcohols and Aldehyde . . . ," 52, (19), 4319-4327 (1987).
S. Torii, et al., J. Org. Chem., "Indirect Electrooxidation of Alcohols and Aldehydes by Using . . . ," 51 (2), 155-161, (1986).
R. A. Sheldon, et al., "Metal-Catalyzed Oxidations of Organic Compounds," Chapter 12, pp. 350-356, Academic Press, New York (1981).
J. March, "Advanced Organic Chemistry," 2nd ed., p. 363, McGraw-Hill Book Co. , New York (1977).

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