Thesis (Ph. D.)--University of Wisconsin--Madison, 1907. / Typescript. With this is bound 6 journal articles: Derivatives of phenyl ether I-V and Phenyl ether and some of its derivatives. Reprinted from the American chemical journal, vol. XXIV, no. 6 (Dec. 1900), p. [525]-529 ; vol. XXVIII, no. 6 (Dec. 1902), p. [486]-490 ; and Journal of the American Chemical Society, vol. XXIII, no. 11 (Nov. 1901), p. [806]-813 ; vol. XXIV, no. 12 (Dec. 1902), p. [1200]-1204 ; vol. XXV, no. 1 (Jan. 1903), p. [60]-68 ; vol. XXXII, no. 10 (Oct. 1910), p. [1285]-1294. Includes bibliography (leaves 64-67) and "Index of new compounds" (leaves 68-69).

Thesis (Ph. D.)--University of Wisconsin--Madison, 1959. / Typescript. Abstracted in Dissertation abstracts, v. 20 (1959) no. 2, p. 507-508. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 38-40).

Thesis (Ph. D.)--University of Chicago. / Also available on the Internet. Also issued online.

A novel preparative method has been discovered in our laboratories which produces hydroxy-substituted phenolic ethers in a simple one-pot process. Initially it was found that 4-hydroxyacetophenone, when oxidized in the presence of ammonium peroxydisulfate and concentrated sulfuric acid in methanol, resulted in 4- methoxyphenol as product in high yield. Being novel, no information about the method was available in the literature, and hence it was our task to study the reaction more extensively. The scope of the reaction was investigated in that different reagents and substrates, as well as alternative oxidants, catalysts and alcohols (or reagents which may be envisaged to behave similarly to alcohols) were used. The studies showed that 4- hydroxy-substituted benzaldehyde and acetophenone, vanillin, fuchsones and stilbenequinones as substrates all successfully afforded the phenolic ether. Other oxidants such as hydrogen peroxide, sodium perborate etc. also afforded the phenolic ether but were less effective. The use of other acids than sulfuric acid resulted in comparable or lower yields of the desired phenolic ether. When the use of alcohols or similar reagents was varied, it was found that methanol, ethanol, benzyl alcohol, allyl alcohol, but-3-en-1-ol, hex-5-en-1-ol and undec-10-en-1-ol all afforded the desired ethers in significant yields. In an investigation to determine how this method may be useful for industrial applications, it was observed that compounds such as 3,5-di-tert-butyl-4-hydroxysubstituted alkenyloxy phenols, having potential application as antioxidant precursors in the polymer industry, may be prepared. Results showed that the reaction became less efficient when the alkenyl chain length was increased. The use of different acids and oxidants, the change of the oxidant:substrate ratio and the addition of a potential lanthanide catalyst did not improve the yield of the desired ether. A mechanism for the reaction was proposed which involved an initial Baeyer-Villiger oxygen insertion step to afford an ester which was hydrolysed in situ to hydroquinone. The remaining oxidant was then involved in oxidizing some of the soformed hydroquinone to benzoquinone. It was then proposed that these two compounds, i.e., hydroquinone and benzoquinone, interacted with each other in solution, forming a charge-transfer complex. According to our proposal, the carbonyl group of the benzoquinone, when complexed with hydroquinone in solution, was then attacked by nucleophilic reagents such as alcohols. Etherification hence resulted as a consequence of this attack. A statistical experimental evaluation and optimization study was then performed which led to a system that produced the phenolic ether, 4-methoxyphenol, in an 86% yield. An analysis of the effects of the reaction parameters on the reaction showed that the reaction temperature and the oxidant:substrate ratio played a major role in deciding the effectiveness of the reaction, while the amount of substrate and acidic catalyst had a much smaller influence on the ether yields.

No description available.

No description available.

No description available.

No description available.

No description available.

No description available.