Nuclear syntheses in the olefin series. II. 1, 4-diolefins

BH Shoemaker, CE Boord

Index: Shoemaker; Boord Journal of the American Chemical Society, 1931 , vol. 53, p. 1507

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Citation Number: 21

Abstract

The nuclear synthesis of unsaturated hydrocarbons previously described3 has been extended to the synthesis of 1, 4-diolefins. This extension has been made possible through the preparation of allylmagnesium bromide by the method described by Gilman and McGl~ mphy.~ The addition of an cr, fl-dibromoalkyl ethyl ether to a slight excess of allylmagnesium bromide in ether solution leads to the formation of an a-allyl-b-bromoalkyl ethyl ether. It ...