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

Chem Pharm Bull (Tokyo). 2018;66(3):303-308. doi: 10.1248/cpb.c17-00897.

Abstract

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°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.

Keywords: benzylating reagent; thermally controllable; triazine.

MeSH terms

  • Alcohols / chemistry
  • Benzene / chemistry*
  • Temperature
  • Triazines / chemistry*

Substances

  • Alcohols
  • Triazines
  • Benzene