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4-Methylcyclohexene is an organic compound consisting of cyclohexene with a methyl group substituent attached to carbon most distant from the alkene group. Two other structural isomers are known: 1-methylcyclohexene and 3-methylcyclohexene.
Most methylcyclohexane is extracted from petroleum but it can be also produced by catalytic hydrogenation of toluene: CH 3 C 6 H 5 + 3 H 2 → CH 3 C 6 H 11. Methylcyclohexane, as a component of a mixture, is usually dehydrogenated to toluene, which increases the octane rating of gasoline.
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1-Methylcyclohexene is used as a probe of the stereochemistry of reactions involving alkenes because it is prochiral and the two sp 2-carbon atoms differ. "Hydrosilylation of Cyclohexene"
Synthesis. It can be produced by a Wittig reaction or a reaction with a Tebbe's reagent from cyclohexanone. [1] [2] [3] It can also be synthesized as a side product ...
Synthesis. 3-Methylcyclohexene is produced from 3-methylcyclohexanone. [1] References This page was last edited on 2 November 2024, at 01:22 (UTC). Text is available ...
Initial synthesis gave a racemic form of the compound using an intramolecular etherification reaction of the alcohol motifs and the double bond. Yamamoto and coworkers report the use of an alternative intramolecular Robinson annulation to provide a straightforward enantioselective synthesis of tetracyclic core of platensimycin.
Benzene is converted to cyclohexylbenzene by acid-catalyzed alkylation with cyclohexene. [6] Cyclohexylbenzene is a precursor to both phenol and cyclohexanone. [7]Hydration of cyclohexene gives cyclohexanol, which can be dehydrogenated to give cyclohexanone, a precursor to caprolactam.