Реакция #2286278
ord-56a6c9fcaa1e44f1ad36d9ef5d71c3d1
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1ТемператураThe reaction mixture was heated
- 2Температураto reflux for 2 d
- 3КонцентрированиеThe reaction mixture was concentrated under vacuum
- 4workup.ADDITIONThe resulting solid was diluted with water (100 mL)
- 5Экстракцияextracted with ethyl acetate (2×75 mL)
- 6workup.ADDITIONThe aqueous layer was acidified to pH=2 by the addition of a 1N aqueous hydrochloric acid solution
- 7Экстракцияwas extracted with ethyl acetate (2×100 mL)
- 8Промывкаwashed with a saturated aqueous sodium chloride solution (2×50 mL)
- 9Сушкаdried with magnesium sulfate
- 10Фильтрацияfiltered
- 11Концентрированиеconcentrated under vacuum
- 12ДругоеThe solid was purified by column chromatography
- 13Промывкаeluted with 15-25% ethyl acetate in petroleum ether
Методика
A suspension of (3,5-dimethyl-4-hydroxy-phenyl)-acetonitrile (4a) (550 mg, 0.003 mol) in water (0.98 mL) was treated with ethylene glycol dimethyl ether (6.6 mL, 0.063 mol) followed by potassium hydroxide (1.34 g, 0.024 mol). The reaction mixture was heated to reflux for 2 d. The reaction mixture was concentrated under vacuum. The resulting solid was diluted with water (100 mL) and extracted with ethyl acetate (2×75 mL). The organic layers were discarded. The aqueous layer was acidified to pH=2 by the addition of a 1N aqueous hydrochloric acid solution and was extracted with ethyl acetate (2×100 mL). The organic layers were combined, washed with a saturated aqueous sodium chloride solution (2×50 mL), dried with magnesium sulfate, filtered and concentrated under vacuum. The solid was purified by column chromatography using silica gel eluted with 15-25% ethyl acetate in petroleum ether to afford (3,5-dimethyl-4-hydroxy-phenyl)-acetic acid (5a) (30 mg, 5%) as a yellow solid; EI(+)-HRMS m/z calcd for C10H12O3 (M+) 180.0786, found 180.0782. Molecular Weight=180.2053; Exact Mass=180.0786