Реакция #52983

ord-4b8ebf0f858447abb7f17f0abe7bc319

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), t-butyl-diphenylsilyl chloride (6.54 g) and imidazole (3.28 g) in DML (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-dimethoxy-1-[(t-butyldiphenylsilyloxy)methyl]benzene. ESMS: m/z 407 (MH+).

Источник

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