Vinyl Cyclohexane Reactions

The method uses a ketone and a methyl vinyl ketone to form an α β unsaturated ketone in a cyclohexane ring by a michael addition followed by an aldol condensation.

Vinyl cyclohexane reactions.

With cyclohexane the average length of the chain hardly exceeds one step and one mole of hydrocarbon reacts with one mole of peroxide. Table 2 reactions of acyclic vinyl triflates and calculated nonclassical int23 22 24 for insertion of cyclohexane into butenyl cation. From wikipedia the free encyclopedia the vinylcyclopropane rearrangement or vinylcyclopropane cyclopentene rearrangement is a ring expansion reaction converting a vinyl substituted cyclopropane ring into a cyclopentene ring. Take off immediately all contaminated clothing.

This procedure is one of the key methods to form fused ring systems. View chapter purchase book synthetic approaches to small and medium size aza heterocycles in aqueous media. 1 vinylcyclohexane permanent link for this species. Use this link for bookmarking this species for future reference.

On a étudié la polymérisation par coordination ionique du vinyl cyclohexane. Use of the information documents and data from the echa website is subject to the terms and conditions of this legal notice and subject to other binding limitations provided for under applicable law the information documents and data made available on the echa website may be reproduced distributed and or used totally or in part for non commercial purposes provided that echa is. 10 17 2016 en english us sds id. Information on this page.

4 vinyl 1 cyclohexene safety data sheet print date. The chemical reaction in this case is a so called ammoximation reaction whereby cyclohexane is reacted with ammonia and hydrogen peroxide at around 90 c in the presence of a titanosilicate catalyst. Des réactions secondaires par exemple isomérisation en composés inactifs comportant une double liaison interne et la transformation du monomère en éthyle cyclohexane se produisent pendant la polymérisation du vinyl cyclohexane sur les catalyseurs complexés organométalliques.