Issue 0, 1968

Reaction between ethyl-lithium and α-methylstyrene in benzene at 30°; formation of 1,3-dimethyl-3-phenyl-1-propylindane

Abstract

Oligo-α-methylstyryl-lithium compounds formed from the reaction between α-methylstyrene and ethyl-lithium decompose slowly in benzene at room temperature to give lithium hydride and substituted indanes. With equimolar concentrations of the two reactants, the main organic product is 1,3-dimethyl-3-phenyl-1-propylindane.

Article information

Article type
Paper

J. Chem. Soc. C, 1968, 3065-3067

Reaction between ethyl-lithium and α-methylstyrene in benzene at 30°; formation of 1,3-dimethyl-3-phenyl-1-propylindane

D. Margerison and V. A. Nyss, J. Chem. Soc. C, 1968, 3065 DOI: 10.1039/J39680003065

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements