A mechanism of the hydrogenation of the double bond in the synthesis of allyl chalcogenides in the hydrazine hydrate-potassium hydroxide system

EN Deryagina, NA Korchevin, NV Russavskaya…

Index: Deryagina; Korchevin; Russavskaya; Grabel'nykh Russian Chemical Bulletin, 1998 , vol. 47, # 9 p. 1827 - 1829

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Citation Number: 6

Abstract

Abstract Allyl halides react with elemental selenium in the N 2 H 4· H 2 O− KOH system to give diallyl chalcogenides and allyl propyl chalcogenides. The latter form only in the presence of oxygen when unsaturated intermediates CH 2= CHCH 2 YK (Y= S and Se), which are soluble in hydrazine hydrate, are hydrogenated with diimide.