Reaction of acetyloxiranes with acetonitrile View Full Text


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Article Info

DATE

1982-08

AUTHORS

O. N. Bubel', I. G. Tishchenko, Yu. L. Ptashnikov

ABSTRACT

2-Acetyloxiranes react with acetonitrile in the presence of equimolar amounts of Lewis acids. It was established that the use of boron trifluoride etherate or sulfuric acid as the catalyst leads to 2,7- and 3,6-diepoxy-1,5-dioxocanes, the use of aluminum trichloride, as well as stannic chloride, leads to the corresponding chlorohydrins, while the use of gaseous boron trifluoride leads to 2-oxazolines in satisfactory yields. It is shown that the reaction is regio- and stereospecific and that the resulting substituted 2-methyl-5-acetyl-2-oxazolines have a cis configuration. More... »

PAGES

773-775

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00506574

DOI

http://dx.doi.org/10.1007/bf00506574

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1012577102


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