Реакция #11327

ord-7128cd1309b044118228bc991451e2cd

Уравнение реакции

O
water
c1nc[nH]n1
1,2,4-triazole
[H-].[Na+]
Sodium hydride
ClC(c1ccccc1)(c1ccccc1)c1ccccc1
tritylchloride
c1ccc(C(c2ccccc2)(c2ccccc2)n2cncn2)cc1
1-trityl-1H-1,2,4-triazole
Выход 47.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGAfter stirring for 1.5 hours at room temperature, to the reaction mixture
  2. 2
    ДругоеThe precipitated crystal was collected by filteration
  3. 3
    Промывкаwashed with water
  4. 4
    workup.DISSOLUTIONdissolved in CHCl3 (800 ml)
  5. 5
    Другоеdried
  6. 6
    ДругоеThe solvent was evaporated
  7. 7
    ДругоеThe obtained residue was chromatographed on silica gel (ethylacetate
  8. 8
    КонцентрированиеThe fraction of the objective was concentrated

Методика

Sodium hydride (60% dispersion in mineral oil, 13.8 g, 345 mmol) was washed with hexane and suspended in DMF (150 ml). At an ice bath temperature, 1,2,4-triazole (total; 20.7 g, 300 mmol) was added thereto in four divisions. After stirring for 30 minutes, to the mixture was added tritylchloride (total; 83.7 g, 300 mmol) in seven divisions and additionally added DMF (50 ml). After stirring for 1.5 hours at room temperature, to the reaction mixture was added water (600 ml). The precipitated crystal was collected by filteration, washed with water, dissolved in CHCl3 (800 ml) and dried. The solvent was evaporated. The obtained residue was chromatographed on silica gel (ethylacetate:CHCl3=1:2, v/v). The fraction of the objective was concentrated to give 1-trityl-1H-1,2,4-triazole (43.9 g). Yield: 47%.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07098201B2uspto-grants-2006_08