PREPARATION OF BORON-SUBSTITUTED CARBORANES BY BORON INSERTION REACTIONS.

Abstract

The boron insertion reaction of Hawthorne was employed in preparing 3-fluoro-, 3-bromo- and 3-diphenylamino-o-carborane. This reaction was further extended to the m-carborane system to produce 2-fluoro- and 2-diphenylamino-m-carborane. 3-Fluoro-o-carborane could be isomerized at 400C to a mixture of 2-fluoro- and 4-fluoro-m-carborane, which was separated by liquid chromatography on a basic alumina column. Likewise, 3-diphenylamino-o-carborane was isomerized, and the 2-diphenylamino- and 4-diphenylamino-m-carborane isomers were separated by the same technique. (Author)

Document Details

Document Type
Technical Report
Publication Date
Mar 01, 1969
Accession Number
AD0683668

Entities

People

  • John S. Roscoe
  • Santad Kongpricha
  • Stelvio Papetti

Tags

DTIC Thesaurus Topics

  • Chromatography
  • Liquid Chromatography

Fields of Study

  • Chemistry

Readers

  • Organic Chemistry