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Aldol Condensation During Hydroformylation

Frequently in the hydroformylation of olefins to aldehydes, a further reaction in varying extent (usually undesired) is aldol condensation. [Pg.62]

There are certain cases, however, where aldol condensation is desired. For instance, by the aldol condensation of butyraldehyde, followed by hydrogenation, one obtains 2-ethylhexanol [893,894,952], a very important [Pg.62]

In this way, more than two thirds of the formed n-butyraldehyde can be converted directly to 2-ethylhexanol. [Pg.63]

The described reactions have been carried to technical production (Esso) under the name Aldox reaction, utilizing a condensation catalyst. Compounds of Zn, Sn, Ti, Zr, Hf, Th, Pb, Cd, Hg, A1 and Cu may also be used for this purpose [709, 715-717, 757, 758, 782-785]. Shell also produces these alcohols in a similar reaction and uses KOH as a condensation catalyst [707]. [Pg.63]

Mg(OCH,)j Pyridine Fe(CO)s 10-2min-i n iso n iso C7H13CHO C7H15CHO 2-Ethyl- 4-methyl- pentanol 2-Ethyl- hexa- nol due [Pg.64]


See other pages where Aldol Condensation During Hydroformylation is mentioned: [Pg.62]    [Pg.63]    [Pg.62]    [Pg.63]    [Pg.132]    [Pg.42]    [Pg.106]    [Pg.150]   
See also in sourсe #XX -- [ Pg.2 , Pg.14 ]




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