N , N′ ‐Dimethylated 6‐(benzyloxy)‐1,3,5‐triazine‐2,4(1 H ,3 H )‐dione (DMBOT) has been developed as a triazinedione‐based, stable solid reagent for acid‐catalyzed O ‐benzylation. The conceptual basis of the design was to fix the core triazinedione skeleton, and the two methyl groups in positions 1 and 3 were introduced to acheive this. The coproduct of DMBOT can be easily removed by simple washing. Various acid‐ and base‐labile alcohols were O ‐benzylated by using DMBOT in the presence of an acid catalyst. In particular, 2,6‐di‐ tert ‐butylpyridinium trifluoromethanesulfonate, which is a mild, stable, and nonhygroscopic acid catalyst, can be used with DMBOT for this reaction. Compared to other reported methods, DMBOT gave better results for several challenging O ‐benzylation reactions under nonbasic conditions.
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Fujita et al. (2016) studied this question.
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