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- W2051697617 abstract "Reaction of phthalic anhydride 1 with benzylidineanilines 2, in equimolar ratio in hot acetic acid, yields N-arylphthalimides 3. Compound 1 reacts with the arylimine part of the Schiff base eliminating benzaldehyde part 4 as the bye-product. This reaction of 1 with 2 is also found to occur with other anhydrides like succinic anhydride 5, maleic anhydride 7 and acetic anhydride 9 resulting in the formation of the corresponding N-arylimides, namely, succinicimide 6, maleicimide 8 and aceticimide 10 respectively. In all the above reactions, the by-product, i.e. benzaldehyde or p-chlorobenzaldehyde can be isolated and characterized as its 2,4-dinitrophenylhydrazone derivative. Probable mechanism for the formation of imides from the corresponding anhydrides and Schiff bases has been suggested." @default.
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- W2051697617 date "2013-08-22" @default.
- W2051697617 modified "2023-09-27" @default.
- W2051697617 title "ChemInform Abstract: Studies on Reactions of Anhydrides with Schiff Bases." @default.
- W2051697617 doi "https://doi.org/10.1002/chin.201337045" @default.
- W2051697617 hasPublicationYear "2013" @default.
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