Abstract
The carbethoxylation product of p-aminoacetophenone with diethyl carbonate by means of sodium amide has been proved to be ethyl p-acetylphenylcarbamate instead of ethyl p-aminobenzoylacetate. Thus the amino group was shown to be more active than the methyl ketonic. group tow ard carbethoxylation. Attempt at further carbethoxylation of this carbamate were unsuccessful.
Degree
MS
College and Department
Physical and Mathematical Sciences; Chemistry and Biochemistry
Rights
http://lib.byu.edu/about/copyright/
BYU ScholarsArchive Citation
Chu, Chao-Yuan, "The carbethoxylation products of p-aminoacetophenone and p-dimethylaminoacetophenone" (1948). Theses and Dissertations. 8189.
https://scholarsarchive.byu.edu/etd/8189
Date Submitted
1948-05-25
Document Type
Thesis
Handle
http://hdl.lib.byu.edu/1877/Letd536
Keywords
Acetophenone
Language
English