The reaction of primary and secondary amides with tetrafluorophthalic or tetrachlorophthalic anhydride gives carboxylic acids in good yield. The reaction is chemoselective in that the amide functionality can be hydrolyzed in the presence of ester groups. We report that the prototypical reaction bet
โฆ LIBER โฆ
Hydrolysis in the absence of bulk water 2. Chemoselective hydrolysis of nitriles using tetrahalophthalic acids
โ Scribed by William D. Rounds; Jefferson T. Eaton; John H. Urbanowicz; Gordon W. Gribble
- Book ID
- 104217838
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 216 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The reaction of nitriles with tetrafluorophthalic or tetrachlorophthalic acid gives carboxylic acids in good yield. The reaction is chemoselective in that the nitrile functionality can be hydrolyzed in the presence of ester groups.
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