Dehydration Reaction of Hydroxamic Acids with Unsaturated Ethers
- 1 January 1962
- journal article
- research article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 35 (1) , 71-75
- https://doi.org/10.1246/bcsj.35.71
Abstract
Dehydration reactions of hydroxamic acids with unsaturated ethers have been studied. The reaction of hydroxamic acids with ethoxyacetylene or methylketene diethylacetal led to the formation of corresponding isocyanates, along with ethyl acetate or ethyl propionate and ethanol, through the intermediate of addition compounds of hydroxamic acids and the dehydrating reagents.Keywords
This publication has 5 references indexed in Scilit:
- Studies on the Beckmann Rearrangement. I. Dehydrations of Aldoximes with Methylketene DiethylacetalThe Journal of Organic Chemistry, 1961
- Dehydration Reactions of Hydroxamic Acids. A New Method for the Preparation of IsocyanatesThe Journal of Organic Chemistry, 1961
- The Dehydration Reactions of AldoximesBulletin of the Chemical Society of Japan, 1960
- The Reactions of Primary Nitroparaffins with Isocyanates1Journal of the American Chemical Society, 1960
- The Dehydration Reactions of Nitroparaffins and AldoximesBulletin of the Chemical Society of Japan, 1960