Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.795458
Title: Some investigations on aromatic structures : (1) Studies in tropolone chemistry; (2) Synthesis of 4:5-dimethylphenanthrene
Author: Scott, Alastair I.
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 1952
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Abstract:
By extension of the method of preparing tropolone by bromination - debydrobromination of oycloheptane-1:2-dione to isopropylcycloheptanediones, alpha-, beta-, and gamma- isopropyltropolones have been prepared and have been shown to be identical with the naturally-occurring alpha-, beta-, and gamma thujaplicins. Some reactions of tropolone have been examined, in particular, the Friedel-Crafts and Reimer-Tiemann reactions. The reduction of tropolone with lithium aluminium hydride has been studied. In the course of an attempt to prepare a gamma-nitrotropolone, cyclodecane-1:2-dione was found to dimerise. The nature of this product has been examined and a structure proposed. An attempted synthesis of gamma-tropolone is also described. PART II. 4:5-Dimethylphenanthrene has been prepared from pyrene by a series of smooth reactions. Ozonolysis of pyrene gave 4-formylphenanthrene-5-carboxylic acid which was reduced to 4:5-bis-hydroxymethyIphenanthrene. Replacement of the hydroxyl groups with bromine followed by the formation of phenanthrene-4:5-diisothioronium dibromide led to the production of 4:5-dimethylphenanthrene. The ultra-violet absorption data of the hydrocarbon and of its intermediates are discussed.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.795458  DOI: Not available
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