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Bromobenzene, conversion to Grignard

Bromobenzaldehyde from aluminum chloride catalyzed bromination of benzaldehyde, 40, 9 Bromobenzene, conversion to Grignard reagent, 41, 91... [Pg.55]

The reaction of ethyl orthoformate and Grignard reagents gives acetals which are hydrolyzed readily by dilute acid to aldehydes. This method has been employed extensively for the preparation of aliphatic and aromatic aldehydes. A study of the optimum conditions has been made, using the conversion of bromobenzene to benzaldehyde as a model synthesis (90%), Comparative studies of various aldehyde syntheses that employ Grignard reagents (methods 154, 166, and 167) show that this one is the most practical however, the possibility of a sudden exothermic reaction limits the size of the run. Longer reaction times at room or reflux tempjerature help overcome this difficulty. Examples of the better preparative procedures are found in those for -hexaldehyde (50%), p-tolualdehyde (TS ), " and phenanthrene-S>-aldehyde (42%)." ... [Pg.598]


See other pages where Bromobenzene, conversion to Grignard is mentioned: [Pg.109]    [Pg.109]    [Pg.381]    [Pg.350]    [Pg.1599]    [Pg.350]    [Pg.212]    [Pg.784]   


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Bromobenzene

Bromobenzene, conversion to Grignard reagent

Bromobenzenes

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