Abstract
WE would like to report a simple method of synthesizing oxetanes. Oxetanes have generally been prepared by a multi-step procedure involving the basic elimination of a halide or acyl radical. The syntheses are involved, and yields are low to fair. Our methods consists of dissolving a diol in a mineral acid, introducing the mixture into a heated solution of base, and distilling off the cyclic ether produced.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Barrow and Searles, J. Amer. Chem. Soc., 75, 1175 (1953).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
SCHMOYER, L., CASE, L. A Simple Synthesis of Oxetanes. Nature 183, 389 (1959). https://doi.org/10.1038/183389a0
Issue date:
DOI: https://doi.org/10.1038/183389a0
This article is cited by
-
Reactions of diols and epoxides
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science (1967)
-
Reactions of diols and epoxides Communication 10. Synthesis of 3-alkyl- and 3-aryl-oxetanes
Bulletin of the Academy of Sciences, USSR Division of Chemical Science (1966)
-
A New Method for the Synthesis of Cyclic Ethers
Nature (1960)