Triketones, from diketone

Sodium carbonate 1,2,3-Triketones from / -diketones via 2-azo-, 2-amino-, 2-diazo-, and 2-hydroxy-1,3-diketones Cyclic trans-tixed -diketones Reduction of water-solubility... 

On the pages which follow, general methods are illustrated for the synthesis of a wide variety of classes of organic compounds including acyl isocyanates (from amides and oxalyl chloride p. 16), epoxides (from reductive coupling of aromatic aldehydes by hexamethylphosphorous triamide p. 31), a-fluoro acids (from 1-alkenes p. 37), 0-lactams (from olefins and chlorosulfonyl isocyanate p. 51), 1 y3,5-triketones (from dianions of 1,3-diketones and esters p. 57), sulfinate esters (from disulfides, alcohols, and lead tetraacetate p. 62), carboxylic acids (from carbonylation of alcohols or olefins via carbonium-ion intermediates p. 72), sulfoxides (from sulfides and sodium periodate p. 78), carbazoles... 

Compartmental ligands (16) are derived from diketonates and triketonates and are usually synthesized from Schiff base reactions of the ketone with a diamine. ... 

PurpurogaHin (5), a red-brown to black mordant dye, forms from electrolytic and other mild oxidations of pyrogaHol (1). The reaction is beHeved to proceed through 3-hydroxy-(9-benzoquinone (2) and 3-hydroxy-6-(3,4,5-trihydroxyphenyl)-(9-benzoquinone (3). The last, in the form of its tautomeric triketonic stmcture, represents the vinylogue of a P-diketone. Acid hydrolysis leads to the formation of (4), foHowed by cyclization and loss of formic acid... 

Aromatic esters may be used to aroylate the dianions derived from 1,3-diketones by reaction with potassium amide (60JOC538). Not only are acetyl and benzoyl acetones suitable for reaction, but alicyclic diketones and 2-hydroxyacetophenone are also acceptable. Cycliz-ation of the triketones occurs in cold sulfuric acid, presumably via the enolic form and the hemiacetal (Scheme 132). 

Ozonolysis of diketone carbonate 417 in methanol afforded an almost quantitative yield of the bicyclic diene triketone hydroxy-ester 418 (119). This remarkable transformation can also be readily explained. Ozonolysis of 417 produces the tetraketone intermediate 419 followed by methanol addition to produce the hemi-ketal 420 which undergoes a retro-Claisen reaction to 421. Then, loss of carbon dioxide from 421 yields 418. Again, 420 could also undergo a Grob type fragmentation to yield 418 directly. 

On treatment with acetic anhydride in pyridine, the yellow tetraketone (68), the yellow triketone (66), and the diketone (67) afforded monoacetyl, diacetyl, and triacetyl derivatives, respectively. All these derivatives contained a tertiary acetoxyl group. However, comparisons of 1H-NMR spectra of the parent ketones with those of the acetyl derivatives indicated that a rearrangement of the molecule or a major conformational change must have occurred. On the basis of extensive H-NMR spectral analysis, structure 69 was proposed for the diacetyl derivative which was derived from the triketone 66. Structure 69 was justified on the basis of conformational arguments. 

Phenylation and arylation have also been performed in bifunctional compounds such as malonates, /1-diketones and /1-ketoesters (Table 8.4). Diethyl malonate was arylated at room temperature affording mixtures of mono- and bis-arylated products, whereas isopropylidene malonate (Meldrum s acid) underwent bis arylation directly. Dimedone, the all carbon analogue of Meldrum s acid, was also mono-and bis-phenylated, with some concomitant O-phenylation [33], Generally, / -diketones show often ambident reactivity but the O-arylated product is normally the minor one an exception was noted in the triketone (PhCO)2CHCOPh which underwent mainly O-phenylation (68%) [33], Several dianions from /1-diketones have been arylated in high yields at the a-position, in a procedure superior to other methods [35]. 

Triketone mono-dithioacetals, 5-diketones prepared from 2-acyl-1,3-dithianes (Section... 

Hauser and co-workers have prepared a number of triketones by (1) acylation of benzoylacetone with aliphatic esters employing lithium amide, (2) by twofold aroylation of acetone with methyl esters using sodium hydride, (3) by aroylation and acylation of aliphatic diketones with potassium amide in liquid ammonia and (4) by aroylation of sodioacetoacetaldehyde in the presence of potassium amide. Disodio- and dipotassiobenzoylacetone are not acylated by ethyl acetate or by phenyl propionate. However, dilithiobenzoylacetone and dilithioacetylacetone with an excess of lithium amide are acylated by aliphatic esters. It is usually more convenient to synthesize 4-pyridones directly from these triketones by cyclization with ethanolic ammonia rather than by way of the intermediate Qpyrone. ... 

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