Master's Theses

Department

Chemistry

Degree Name

Master of Science (MS)

Abstract

A method for the preparation of 2-amino-4-phenylthiazoles and its derivatives has been performed. Considering that some previous methods were time consuming, a way has been found to prepare these compounds in reasonable amounts of time. The need of finding a convenient way of brominating acetophenones was investigated. The use of selective bromination with copper (II) bromide offered a convenient method so that compounds could be brominated without the need of isolating the lachromatory products. The products obtained from this type of bromination were then reacted with thiourea to arrive at the aminothiazole.

Keywords

Chemicals, Acetophenone, Bromination, Aminothiazoles, Experiments, Heterocyclic chemistry

Advisor

Dr. James H. McMechan

Date of Award

Summer 1972

Document Type

Thesis - campus only access

Rights

© The Author(s)

Comments

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