110466-47-2

Upstream product

• 5650-07-7 3-methyl-1-phenyl-but-2-en-1-one 
• 128260-03-7 4,4-ethylenedioxy-2-methyl-4-phenylbutan-2-ol 
• 128259-95-0 3,3-dimethyl-4-nitro-1-phenyl-pentan-1-one 
• 110466-43-8 3,3-dimethyl-1-phenylpentane-1,4-dione 

Relevant academic research and scientific papers

Synthesis and Chemistry of Azolenines. Part 16. Preparation of both 3H- and 2H-Pyrroles from 2,2-Disubstituted 1,4-Diketones via the Paal-Knorr Reaction, and Isolation of Intermediate 2-Hydroxy-3,4-dihydro-2H-pyrroles

Treatment of 2,2-disubstituted 1,4-diketones (1) with liquid ammonia gives high yields of isolable isomeric 2-hydroxy-3,4-dihydro-2H-pyrroles (10) and (11), many of which may be dehydrated to 3H-pyrroles (2) together, in certain cases, with isomeric methylene-pyrrolines (14) and (15).When heated in acetic acid with ammonium acetate, the diketones (1) yield 2H-pyrroles (18), sometimes in admixture with 3H-pyrroles (2) from which they are formed by rearrangement.The diketones (1), including some novel examples, are prepared from nitro-ketones (6) by the Nef reaction, as well as other methods.

Novel Synthesis of 3H-Pyrroles, and Novel Intermediates in the Paal-Knorr 1H-Pyrrole Synthesis: 2-Hydroxy-3,4-dihydro-2H-pyrroles from 1,4-Diketones and Liquid Ammonia

Reaction of 2,2-dimethyl-1,4-diketones with liquid ammonia gives high yields of isolable 2-hydroxy-3,4-dihydro-2H-pyrroles (3) and (5) which are readily dehydrated to give separable mixtures of 3H-pyrroles and methylenedihydropyrroles, while less-substituted 1,4-diketones give analogous hydroxy-compounds (4) and (6) which are hitherto-unsuspected intermediates in the Paal-Knorr 1H-pyrrole synthesis.