Реакция #684971
ord-61e35bb18f3f4c16ac066b8c62c662e6
Уравнение реакции
Trifluoroacetic acid
compound
2-(4-Butylbenzyl)-3-(methoxymethoxy)pyridine
sodium hydrogencarbonate
ethyl acetate
→
title compound
Выход 88.8%
2-(4-Butylbenzyl)-3-pyridinol
Выход 88.8%
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Промывкаthe reaction mixture was washed with saturated brine
- 2Концентрированиеconcentrated under reduced pressure
- 3ДругоеThe residue was purified by silica gel column chromatography
Методика
Trifluoroacetic acid (1 ml) was added to a solution of the compound of Example B229 (256 mg, 0.849 mmol) in methylene chloride (5 ml), and this reaction mixture was stirred at room temperature overnight. After a saturated aqueous sodium hydrogencarbonate solution and ethyl acetate were added, the reaction mixture was washed with saturated brine and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (182 mg).