Реакция #487568

ord-0800fa9387b9482a9a736d73d24b8c44

Уравнение реакции

Clc1ccnc2[nH]ccc12
4-chloro-1H-pyrrolo[2,3-b]pyridine
C[Si](C)(C)CCOCCl
[β-(trimethylsilyl)ethoxy]methyl chloride
CN(C)C=O
N,N-dimethylformamide
[H-].[Na+]
sodium hydride
C[Si](C)(C)CCOCn1ccc2c(Cl)ccnc21
orange oil
Выход 112.5%
C[Si](C)(C)CCOCn1ccc2c(Cl)ccnc21
4-Chloro-1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridine
Выход 112.5%

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеpartitioned between ethyl acetate and water (×2)
  2. 2
    Промывкаthe organic layer was washed with sat. NaCl
  3. 3
    ДругоеThe organic layer was then dried under vacuum

Методика

To a 0° C. solution of 4-chloro-1H-pyrrolo[2,3-b]pyridine (0.50 g, 0.0033 mol) and [β-(trimethylsilyl)ethoxy]methyl chloride (0.75 mL, 0.0043 mol) in N,N-dimethylformamide (5 mL, 0.06 mol) was added sodium hydride (0.17 g, 0.0043 mol). The resulting mixture was stirred overnight and partitioned between ethyl acetate and water (×2), and the organic layer was washed with sat. NaCl. The organic layer was then dried under vacuum to produce 1.05 g of an orange oil which was chromatographed with 15% ethyl acetate/hex to give 830 mg of a colorless oil (89.6% yield).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08741895B2uspto-grants-2014_06