Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Vinylcyclo-hexane

In continuing the study of hydrosilation of alkylcyclohexenes, Benkeser et al. (13) studied in detail the addition of Cl3SiH (with H2PtCl6) to 1-, 3-, and 4-ethylcyclohexenes, as well as to ethylidene- and vinylcy-clohexenes. With an olefin/Cl3SiH ratio of 1/1.9 at reflux, vinylcyclo-hexane gave a 68% yield of adduct in 0.5 hours. The other olefins required much more time e.g., 96 hours was needed to achieve 83% yield from 3-ethylcyclohexene. Each olefin made the same adduct— C6HnCH2CH2SiCl3—and recovered olefins were mixtures of all possible... [Pg.424]

Traditional Ziegler-Natta and metallocene initiators polymerize a variety of monomers, including ethylene and a-olefins such as propene, 1-butene, 4-methyl-1-pentene, vinylcyclo-hexane, and styrene. 1,1-Disubstituted alkenes such as isobutylene are polymerized by some metallocene initiators, but the reaction proceeds by a cationic polymerization [Baird, 2000]. Polymerizations of styrene, 1,2-disubstituted alkenes, and alkynes are discussed in this section polymerization of 1,3-dienes is discussed in Sec. 8-10. The polymerization of polar monomers is discussed in Sec. 8-12. [Pg.682]

The isomerization polymerization with material transport makes it possible to distinguish between a polymerization by hydride shift as in 3-methylbutene-l (or 4-methylpentene-l, 4-methylhexene-l, or vinylcyclo-hexane),... [Pg.645]

The influence of steric factors on reactivity and on selectivity has been discussed for the catalysis, by a variety of phosphine complexes of ruthenium, iridium, and platinum, of the isomerization of 4-vinylcyclo-hexane. Titanium tetra-( - )-menthoxide plus tri-isobutylaluminium catalyse stereoselective isomerization of racemic alk-l-enes. ... [Pg.287]

A second major reaction of oxaspiropentanes as reactive epoxides is their elimination to form vinylcyclopropanols 29,49,62). A rapid elimination to vinylcyclo-propanols occurs when the oxaspiropentanes are exposed to lithium dialkylamides in hexane or pentane as exemplified in Eq. 34 and Table 4. [Pg.31]

Cyclohexane (main product), cyclohexene, vinylcyclohexane, vinylcyclo 100 hexane oligomers, methane, ethane, ethylene, propane, propylene, butane, butylene, hydrogen... [Pg.487]


See other pages where Vinylcyclo-hexane is mentioned: [Pg.427]    [Pg.228]    [Pg.27]    [Pg.61]    [Pg.277]    [Pg.427]    [Pg.228]    [Pg.27]    [Pg.61]    [Pg.277]    [Pg.1350]   
See also in sourсe #XX -- [ Pg.228 ]




SEARCH



© 2024 chempedia.info