Реакция #52986

ord-5a5ba54c17ac44b8bce09720bb95188c

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеDMF was evaporated
  2. 2
    Другоеthe residue was purified by column chromatography (silica gel; eluent: hexane to hexane/EtOAc 20% )

Методика

A mixture of 3,5-dimethoxybenzyl alcohol (4.0 g), tert-butyl-diphenylsilyl chloride (6.54 g) and imidazole (3.28 g) in DMF (60 mL) was stirred at room temperature for 24 h. DMF was evaporated and the residue was purified by column chromatography (silica gel; eluent: hexane to hexane/EtOAc 20% ) to yield 8.5 g of 3,5-dimethoxybenzyl tert-butyldiphenylsilyl ether. ESMS: m/z 407 (MH+).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06855843B2uspto-grants-2005_02