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Aromatization of petroleum hydrocarbons. Synthesis of cyclopentenediones (a summary).
by Ronald H. Blizzard
| Institution: | McGill University |
|---|---|
| Department: | Department of Chemistry. |
| Degree: | PhD |
| Year: | 1942 |
| Keywords: | Chemistry. |
| Posted: | |
| Record ID: | 1582423 |
| Full text PDF: | http://digitool.library.mcgill.ca/thesisfile125904.pdf |
The feasibility of producing toluene by the aromatization of paraffins and naphthenes has been reinvestigated. The preparation of chromium oxide-alumina catalysts has been improved and the optimum conditions for the aromatization of pure n-heptane, methylcyclohexane, heptenes, enfi selected fractions of a Turner Valley naphtha have been determined. A simplified catalysis apparatus and a new type of stillhead are described. Data is given for the preparation of isomeric heptenes and heptane from heptanol-2, and for a close fractionation of a Turner Valley naphtha. The Gabriel-Nathanson Rearrangement of benzalmaleide into 2-phenylcyclopentenedione-1, 3, of α, β- diphenyl-γ-benzalcrotonolactone into triphenylcyclopentenedione, and of benzalphthalide into 2-phenylindandione-1,3 has been investigated in part.
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