Reactions of N-Aminophthalimide With Electrophiles. II. Preparation and Properties of Araldehyde Hydrazones
N-Aminophthalimide (I) reacted with a variety of aromatic aldehydes to give the related arylideneaminophthalimides (III-X), although typical ketones such as acetone and benzophenone did not under the specific conditions employed.Catalytic reduction of benzylideneaminophthalimide (III) led to N-benzylaminophthalimide (XI), a stable acid-free precursor of benzylhydrazine.
Hearn, Michael J.,Lucero, Elena R.
p. 1537 - 1539
(2007/10/02)
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