Catalytic asymmetric epoxidation
AssigneeMassachusetts Institute of Technology
InventorsRobert M. Hanson, Soo Y Ko, Karl B. Sharpless
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Abstract
Improved method for epoxidation of ethylenic alcohols is provided employing catalytic amounts of a titanium-glycol catalyst and a peroxide under mild conditions which provide for the continuous maintenance of an anhydrous medium during catalyst formation and during the course of the reaction. Conveniently, molecular sieves may be employed.
Claims9
In a method employing a titanium chiral glycol alkoxide catalyst, an olefinic alcohol, where the olefin is separated from the carbinol carbon atom by from 0 to 1 carbon atom, and an organic hydroperoxide in an inert dry medium under mild conditions below about 30.degree. C., whereby the olefin is asymmetrically epoxidized, the improvement which comprises:
- epoxidizing the olefin in the presence of from about 1-25 mol percent based on olefin of said catalyst under conditions where any water formed is continuously removed from the reaction mixture by means of a dehydrating agent.
In a method for preparing glycidol from allyl alcohol, wherein a titanium chiral glycol alkoxide catalyst is combined with allyl alcohol and a hydroperoxide in an inert anhydrous halohydrocarbon medium under mild conditions at a temperature in the range of about -100.degree. to 20.degree. C., whereby said allyl alcohol is epoxidized to glycidol, the improvement which comprises:
- preparing said catalyst in the presence of activated molecular sieves;
- and
- including in said inert medium in an amount sufficient to adsorb any water which is formed, activated molecular sieves, wherein said catalyst is present in from about 1-25 mol percent based on olefin.
Dependencies are inferred from the claim text.