It was stated that the action of heated sodium hydroxide upon ?, ? `-dichlorodiethyl ether produced a liquid boiling at 39 �C ( among other identified products ) . ( Major, 1935 ) However, in a subtly modified process Hibbert et al . reported the isolation of a product boiling at 34-35 �C, " divinyl ether ".
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This substance produced results placing it between diethyl ether and divinyl ether both in terms of toxicity and speed of induction and recovery, producing promising results similar to V . A . M . ( Grosskreutz, Davis 1956 ) Despite much simpler synthesis ( vinylization of ethanol with acetylene ) ethyl vinyl ether didn't enter widespread use in anasthetics, as superior halogenated ethers replaced it shortly after its first trials.
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