Pavey, Andrew
2015.
The novel rearrangement of 1-acetyl-1-methylcyclohexa-2,5-diene.
MPhil Thesis,
Cardiff University.
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Abstract
This thesis describes the results of the research into the novel rearrangement of 1-acetyl-1-methylcyclohexa-2,5-diene under basic conditions. The rearrangement involves the migration of an acetyl group around the cyclohexadiene ring. The rearrangement occurs via a cyclopropane intermediate, to produce a mixture of two isomers. The study involves calculations that evaluate the feasibility of the proposed mechanism. This is coupled with the experimental data for the rearrangement with a range of alkylating agents. Chapter 1 presents a description of previous work carried out by the Elliott group and how the novel rearrangement of 1-acetyl-1-methylcyclohexa-2,5-diene was discovered. The proposed mechanism for the rearrangement is discussed which sets the stage for the work discussed in chapter 2. Chapter 2 presents a review of Birch reduction chemistry. This was utilised as a synthetic route to produce 1-acetyl-1-methylcyclohexa-2,5-diene which is used as the starting material for rearrangement reactions. Chapter 3 discusses the rearrangement reaction of 1-acetyl-1-methylcyclohexa-2,5-diene with a range of alkylating agents. It is followed by a computational study that evaluates the feasibility of the proposed mechanism. Chapter 4 describes the brief evaluation of Na-SG as a method for partial reduction of aromatic compounds.
Item Type: | Thesis (MPhil) |
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Date Type: | Submission |
Status: | Unpublished |
Schools: | Chemistry |
Subjects: | Q Science > QD Chemistry |
Date of First Compliant Deposit: | 10 June 2016 |
Last Modified: | 18 Jul 2017 01:30 |
URI: | https://orca.cardiff.ac.uk/id/eprint/91722 |
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