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Nitrosation of methyl ethyl ketone

Biacetyl is produced by the dehydrogenation of 2,3-butanediol with a copper catalyst (290,291). Prior to the availabiUty of 2,3-butanediol, biacetyl was prepared by the nitrosation of methyl ethyl ketone and the hydrolysis of the resultant oxime. Other commercial routes include passing vinylacetylene into a solution of mercuric sulfate in sulfuric acid and decomposing the insoluble product with dilute hydrochloric acid (292), by the reaction of acetal with formaldehyde (293), by the acid-cataly2ed condensation of 1-hydroxyacetone with formaldehyde (294), and by fermentation of lactic acid bacterium (295—297). Acetoin [513-86-0] (3-hydroxy-2-butanone) is also coproduced in lactic acid fermentation. [Pg.498]


See also in sourсe #XX -- [ Pg.10 , Pg.22 ]

See also in sourсe #XX -- [ Pg.10 , Pg.22 ]

See also in sourсe #XX -- [ Pg.10 , Pg.22 ]

See also in sourсe #XX -- [ Pg.10 , Pg.22 ]

See also in sourсe #XX -- [ Pg.10 , Pg.22 ]

See also in sourсe #XX -- [ Pg.10 , Pg.22 ]

See also in sourсe #XX -- [ Pg.10 , Pg.22 ]




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Ethyl ketones

Methyl ethyl ketone

Nitrosates

Nitrosating

Nitrosation

Nitrosation of ketones

Of ethyl methyl ketone

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