Реакция #41148

ord-9b10de844b7a4ec5a9ee586191ff0421

Уравнение реакции

COC(=O)c1cnn(C(C)(C)C)c1CBr
5-bromomethyl-1-tert-butyl-1H-pyrazole-4-carboxylic acid methyl ester
CC[O-].[Na+]
sodium ethoxide
CCO
ethanol
CCOCc1c(C(=O)OCC)cnn1C(C)(C)C
1-tert-butyl-5-ethoxymethyl-1H-pyrazole-4-carboxylic acid ethyl ester
Выход 51.0%

Условия реакции

Температура
90°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеAt this time, the reaction was concentrated in vacuo
  2. 2
    ДругоеThe residue was partitioned between ethyl acetate (75 mL) and water (50 mL)
  3. 3
    ПромывкаThe organics were washed with a saturated aqueous sodium bicarbonate solution (1×50 mL)
  4. 4
    Сушкаa saturated aqueous sodium chloride solution (1×50 mL), dried over magnesium sulfate
  5. 5
    Фильтрацияfiltered
  6. 6
    Концентрированиеconcentrated in vacuo

Методика

A solution of 5-bromomethyl-1-tert-butyl-1H-pyrazole-4-carboxylic acid methyl ester (220 mg, 0.79 mmol) in ethanol (4.0 mL, 0.2M) was treated with sodium ethoxide (65.4 mg, 0.96 mmol). The reaction mixture was warmed to 90° C. where it was stirred for 2.5 h. At this time, the reaction was concentrated in vacuo. The residue was partitioned between ethyl acetate (75 mL) and water (50 mL). The organics were washed with a saturated aqueous sodium bicarbonate solution (1×50 mL) and a saturated aqueous sodium chloride solution (1×50 mL), dried over magnesium sulfate, filtered and concentrated in vacuo to afford 1-tert-butyl-5-ethoxymethyl-1H-pyrazole-4-carboxylic acid ethyl ester (102.8 mg, 51%) as an orange oil. The material was used without further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07728029B2uspto-grants-2010_06