反应 #1519121

ord-2d2116e22de8483d8fa93674a653ca22

反应方程式

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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Reaction mixture
  2. 2
    其他The resultant precipitate is removed by filtration
  3. 3
    洗涤washed thoroughly with dry benzene
  4. 4
    浓缩The filtrate is gently concentrated
  5. 5
    其他to avoid evaporating the highly volatile product

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07612059B2uspto-grants-2009_11