The addition of HCl and HBr to 1-phenyl-4-t-butylcyclohexene. The isolation of the stereomers cis- and trans-1-chloro-1-phenyl-4-t-butylcyclohexane and the stereochemistry of the addition process

K. Darrell Berlin; Reginald O. Lyerla; Don E. Gibbs; J. Paul Devlin

doi:10.1039/C29700001246

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The addition of HCl and HBr to 1-phenyl-4-t-butylcyclohexene. The isolation of the stereomers cis- and trans-1-chloro-1-phenyl-4-t-butylcyclohexane and the stereochemistry of the addition process

K. Darrell Berlin, Reginald O. Lyerla, Don E. Gibbs and J. Paul Devlin

Abstract

Solid geometrical isomers have been isolated from the reaction of 1-phenyl-4-t-butylcyclohexene and HCl, which is shown to be a syn-addition process.

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DOI: https://doi.org/10.1039/C29700001246
Article type: Paper

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J. Chem. Soc. D, 1970, 1246-1247

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The addition of HCl and HBr to 1-phenyl-4-t-butylcyclohexene. The isolation of the stereomers cis- and trans-1-chloro-1-phenyl-4-t-butylcyclohexane and the stereochemistry of the addition process

K. D. Berlin, R. O. Lyerla, D. E. Gibbs and J. P. Devlin, J. Chem. Soc. D, 1970, 1246 DOI: 10.1039/C29700001246

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Journal of the Chemical Society D: Chemical Communications

The addition of HCl and HBr to 1-phenyl-4-t-butylcyclohexene. The isolation of the stereomers cis- and trans-1-chloro-1-phenyl-4-t-butylcyclohexane and the stereochemistry of the addition process

Abstract

Article information

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The addition of HCl and HBr to 1-phenyl-4-t-butylcyclohexene. The isolation of the stereomers cis- and trans-1-chloro-1-phenyl-4-t-butylcyclohexane and the stereochemistry of the addition process

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