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Alumina as reagent. The one-step conversion of benzyl chloride and bromide into dibenzyl ether

✍ Scribed by George Hondrogiannis; Lay Choo Tan; Richard M. Pagni; George W. Kabalka; Sherry Herold; Emily Ross; James Green; Michael McGinnis


Publisher
Elsevier Science
Year
1994
Tongue
French
Weight
276 KB
Volume
35
Category
Article
ISSN
0040-4039

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✦ Synopsis


Ben@ chloride and bromide react with alumina via a two-step mechanism to produce dibenzyl ether in good yield. Chemisorbed benzyloxy is the other major product of the reactions.

The surfaces of inorganic oxides such as alumina, silica gel, clays, and zcolites provide unusual environments for chemical transformations.'

Alumina is particularly interesting in this regard because its surface is polaf and contains immobile, catalytic BrBnsted and Lewis acidic (OH, Al+') and basic