Реакция #657257

ord-852f47be86574ff68e08c58c5bd293f0

Уравнение реакции

CCOCc1cnn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c1
1-trityl-4-ethoxymethylpyrazole
CCOCc1cn[nH]c1
4-ethoxymethylpyrazole
Выход 44.0%

Реагенты

Нет

Растворители

Условия реакции

Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added to the resulting solution
  2. 2
    ТемператураAfter cooling to room temperature
  3. 3
    Фильтрацияthe reaction mixture was filtered
  4. 4
    Промывкаwashed with dichloromethane
  5. 5
    Экстракцияextracted with dichloromethane
  6. 6
    Сушкаdried over MgSO4
  7. 7
    Другоеthe solvent was evaporated under vacuum

Методика

1-trityl-4-ethoxymethylpyrazole (1.800 g, 4.88 mmol) was dissolved in a mixture of ethanol/acetone (15 ml/5 ml) and 30 mL of 2N HCl was added to the resulting solution. The mixture was heated at 80° C. for 2 h. After cooling to room temperature, the reaction mixture was filtered and washed with dichloromethane. The aqueous layer was basified with 2N NaOH and extracted with dichloromethane. The organic layers were combined, dried over MgSO4 and the solvent was evaporated under vacuum yielding compound 4-ethoxymethylpyrazole as a white oil. Yield: 44% (270 mg, 2.14 mmol).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09023315B2uspto-grants-2015_05