Accession Number : AD0701102
Title : SYNTHETIC APPLICATIONS OF AROMATIC DESILYLATION AND DESTANNYLATION.
Descriptive Note : Final rept.,
Corporate Author : SUSSEX UNIV BRIGHTON (ENGLAND)
Personal Author(s) : Barlett,E. H. ; Eaborn,C. ; Walton,D. R. M.
Report Date : OCT 1969
Pagination or Media Count : 14
Abstract : Two novel electrophilic displacement reactions have been discovered and their scope as synthetic methods examined. The first provides a useful route to aryl nitroso compounds and involves reaction of aryltrimethyl-silanes or -stannanes with nitrosyl chloride (no catalyst being necessary with the stannanes): NOCl + XC6H4MMe3 yields XC6H4NO. The second provides a useful route to aryl cyanides, and involves reaction of the aryltrimethyl -silanes or -stannanes with cyanogen chloride in the presence of aluminium chloride: ClCN + XC6H4MMe3 yields (over AlCl3) XC6H4CN. In both cases the best yields are obtained from the organotin compounds, with methylene chloride as solvent. Reactions with cyanogen bromide take a different course: BrCN + PhSnMe3 yields PhBr + Me3SnCN. Arenesulphonyl chlorides have been found to react with bistrimethylsilylacetylene under Friedel Crafts conditions, and this provides a novel synthesis of ethynyl sulphones: XC6H4SO2Cl + Me3SiCCSiMe3 yields (over AlCl3) Me3SiCCSO2C6H4X. (Author)
Descriptors : (*NITROSO COMPOUNDS, SYNTHESIS(CHEMISTRY)), (*NITRILES, SYNTHESIS(CHEMISTRY)), (*SILANES, CHEMICAL REACTIONS), DISPLACEMENT REACTIONS, TIN COMPOUNDS, METALORGANIC COMPOUNDS, CYANIDES, HALIDES, HALOGENATED HYDROCARBONS, AROMATIC COMPOUNDS, GREAT BRITAIN
Subject Categories : Organic Chemistry
Distribution Statement : APPROVED FOR PUBLIC RELEASE