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Development of Triazine-Based Benzylating Reagents Possessing t-Butyl Group on the Triazine Core: Thermally Controllable Reagents for the Initiation of Reaction

机译:在三嗪芯上具有叔丁基的三嗪基苄晶试剂的研制:可热可控试剂进行反应的启动

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摘要

Benzylating reagents, 4-(4,6-di-t-butyl-1,3,5-triazin-2-yl)-4-benzylmorpholinium triflate, and related derivatives have been developed. The reagents release benzyl triflate as a benzyl cation equivalent upon heating the solution to 40 degrees C under neutral conditions. The O-benzylation of alcohols using a stoichiometric amount of these reagents afforded corresponding benzyl ethers in good to high yields. This was due to the presence of a bulky t-butyl group on the triazine ring of these reagents that prevents the consumption of benzyl triflate via a side reaction with a morpholinotriazine derivative.
机译:已经开发了苄晶试剂,4-(4,6-二叔丁基-1,3,5-三嗪-2-基)-4-苄基胆胆糖酸酯和相关衍生物。 试剂在中性条件下将溶液加热至40℃时,试剂释放苄基作为苄基阳离子等同物。 使用化学计量的这些试剂的醇的O-苄基化得到相应的苄基醚,良好至高产率。 这是由于这些试剂的三嗪环上存在庞大的叔丁基,其防止通过与吗啉二嗪衍生物的副反应来消耗苄基Triflate。

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