In the first of three syntheses vanillin is converted to benzoyl vanillic acid, then successively to the acyl chloride, cyanide with subsequent reduction to the amine.
The second method involves the synthesis of vanillin cyanohydrin followed by reduction to the amine.
The third method involves the Fries rearrangement of guaiacol acetate followed by bromination of the acetophenone and conversion to the amine. / Science, Faculty of / Chemistry, Department of / Graduate
| Identifer | oai:union.ndltd.org:UBC/oai:circle.library.ubc.ca:2429/41901 |
| Date | January 1947 |
| Creators | Hamilton, John Kelvin |
| Publisher | University of British Columbia |
| Source Sets | University of British Columbia |
| Language | English |
| Detected Language | English |
| Type | Text, Thesis/Dissertation |
| Rights | For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use. |
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