Intramolecular Alkylation During the Reaction of Aryldiazonium Salts
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Authors
Makowski, David N.
Issue Date
1975
Type
Thesis
Language
en_US
Keywords
Alternative Title
Abstract
The purpose of this SIP was to study the influence of reaction conditions upon the intramolecular alkylation of aryldiazonium salts. Intramolecular alkylation occurred most readily in a cold, acidic medium. It also occurred in an aprotic medium, but in only modest yield. With the introduction of HCl by means of the hydrochloride 2,5-di-i-butyl-aniline hydrochloride the yield of 2-methyl-5-i-butylbenzene in the aprotic medium doubled.
Description
47 p.
Citation
Publisher
Kalamazoo College
License
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