Реакция #1519121

ord-2d2116e22de8483d8fa93674a653ca22

Уравнение реакции

C[Si](C)(C)Cl
TMSCl
c1c[nH]nn1
1H-1,2,3-triazole
C[Si](C)(C)c1c[nH]nn1
TMS-triazole

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеReaction mixture
  2. 2
    ДругоеThe resultant precipitate is removed by filtration
  3. 3
    Промывкаwashed thoroughly with dry benzene
  4. 4
    КонцентрированиеThe filtrate is gently concentrated
  5. 5
    Другоеto avoid evaporating the highly volatile product

Методика

To a solution of 1H-1,2,3-triazole (4.98 g, 72.10 mmol, 1 equiv.) in dry benzene (145 mL) at rt under nitrogen, is added TEA (11.05 mL, 79.31 mmol, 1.1 equiv.) followed by the dropwise addition of TMSCl (9.15 mL, 72.10 mmol, 1 equiv.). A white precipitate develops. Reaction mixture is stirred at rt under nitrogen for 1 hour. The resultant precipitate is removed by filtration and washed thoroughly with dry benzene. The filtrate is gently concentrated to avoid evaporating the highly volatile product to give a quantitative yield of TMS-triazole with a trace of benzene.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07612059B2uspto-grants-2009_11