Реакция #50880

ord-1cffddb7e50e4d50a76e4abb31db29ea

Уравнение реакции

O=Cc1cccc(CO)c1
3-hydroxymethylbenzaldehyde
CC(C)(C)[Si](Cl)(c1ccccc1)c1ccccc1
t-butylchlorodiphenyl silane
c1cc(N2CCCC2)ccn1
4-pyrrolidinopyridine
CC(C)(C)[Si](OCc1cccc(C=O)c1)(c1ccccc1)c1ccccc1
title compound
CC(C)(C)[Si](OCc1cccc(C=O)c1)(c1ccccc1)c1ccccc1
3-t-butyldiphenylsilyloxymethylbenzaldehyde

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe solution was quenched with 25% ammonium acetate
  2. 2
    Экстракцияextracted with ethyl acetate, which
  3. 3
    Промывкаwas washed with brine (2×)
  4. 4
    Сушкаdried over sodium sulfate
  5. 5
    Фильтрацияfiltered
  6. 6
    Другоеevaporated to dryness
  7. 7
    ДругоеPurification by flash chromatography

Методика

To a solution of 3-hydroxymethylbenzaldehyde (step 1) (3 g) in methylene chloride (15 mL) and triethylamine (4.1 mL) was slowly added t-butylchlorodiphenyl silane (8 mL). Finally, a few mgs of 4-pyrrolidinopyridine was added as a catalyst. The reaction mixture was stirred overnight at room temperature (R.T.). The solution was quenched with 25% ammonium acetate and extracted with ethyl acetate, which was washed with brine (2×), dried over sodium sulfate, filtered and evaporated to dryness. Purification by flash chromatography, using 4% ethyl acetate in hexane afforded the title compound.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05428171uspto-grants-1995_06