Реакция #955937
ord-7317d8f3f7bd471f83b179f209684c86
Уравнение реакции
Реагенты
Условия реакции
Обработка
- 1Другоеgiving a red color
- 2Другоеquenched upon the addition of aq. HCl (1M, 50 mL)
- 3ЭкстракцияThe crude product was extracted with ether
- 4Промывкаthe combined organic layers were successively washed with water and brine
- 5Сушкаdried over MgSO4
- 6Фильтрацияfiltered
- 7Другоеevaporated
- 8ДругоеThe residue was purified on silica gel (Eluent: 30% EtOAc in hexanes)
Методика
To a solution of methyl 4-chloro-2-methoxybenzoate (example 18d) (4.16 g, 20.8 mmol) in THF (120 mL) and NMP (12 mL) was added under inert atmosphere Iron (III) acetylacetonate (398 mg, 1.17 mmol) giving a red color. Then EtMgBr (29 ml of 1M solution in ether) was added dropwise under vigorous stirring. The mixture turned dark brown and then violet and then was stirred for 15 more min. The reaction was diluted with ether and quenched upon the addition of aq. HCl (1M, 50 mL). The crude product was extracted with ether and the combined organic layers were successively washed with water and brine, dried over MgSO4, filtered and evaporated. The residue was purified on silica gel (Eluent: 30% EtOAc in hexanes) to give methyl 4-ethyl-2-methoxybenzoate (2.01 g, 50%) as an oil. 1H NMR (300 MHz, dMSO): δ 1.20-1.22(t, 3H), 2.65-2.7 (dd, 2H), 3.9 (s, 3H), 6.8 (s, 1H), 6.97 (m, 1H), 7.7 (m, 1H).