4-vinyl-1-cyclohexene
4-Vinylcyclohexene is an organic compound consisting of a vinyl group attached to the 4-position of the cyclohexene ring. It is a colorless liquid. Although chiral, it is used mainly as the racemate. It is a precursor to vinylcyclohexene dioxide.
Article
3 sectionsContents
- Production
- Safety
- References
4-Vinylcyclohexene is an organic compound consisting of a vinyl group attached to the 4-position of the cyclohexene ring. It is a colorless liquid. Although chiral, it is used mainly as the racemate. It is a precursor to vinylcyclohexene dioxide.
==Production== It is produced by buta-1,3-diene dimerization in a Diels-Alder reaction. The reaction is conducted at 110 - 425 °C at pressures of 1.3 - 100 MPa in the presence of a catalyst. A mixture of silicon carbide and salts of copper or chromium comprises the catalyst. A competing product is 1,5-cyclooctadiene. 500 px|1,3-Butadiene undergoes a Diels-Alder cycloaddition reaction to form 4-vinylcyclohexane. In North America this is produced by Nippon Chemical Texas Inc. in Pasadena, TX.