## Abstract In the reaction of oximes I with ethoxyethyne II at 75‐90° orthoesterlike products III are formed. Some aldoximes, however, are dehydrated to nitriles. The results are summarized in Table I.
Chemistry of acetylenic ethers XXXV. Reactions of alkali metal derivatives of ethoxyethyne and of ethylthioethyne with epichlorohydrin
✍ Scribed by G. Vollema; J. F. Arens
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 244 KB
- Volume
- 78
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
The reaction between epichlorohydrin and ethylthioethynyl‐lithium affords the enynol V and furfuryl ethyl sulphide VI. The same reaction with ethoxyethynyl‐lithium, however, produces the epoxy compound VII.
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