Реакция #955937

ord-7317d8f3f7bd471f83b179f209684c86

Уравнение реакции

C[CH2][Mg+].[Br-]
EtMgBr
COC(=O)c1ccc(Cl)cc1OC
methyl 4-chloro-2-methoxybenzoate
CCc1ccc(C(=O)OC)c(OC)c1
methyl 4-ethyl-2-methoxybenzoate
Выход 50.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеgiving a red color
  2. 2
    Другоеquenched upon the addition of aq. HCl (1M, 50 mL)
  3. 3
    ЭкстракцияThe crude product was extracted with ether
  4. 4
    Промывкаthe combined organic layers were successively washed with water and brine
  5. 5
    Сушкаdried over MgSO4
  6. 6
    Фильтрацияfiltered
  7. 7
    Другоеevaporated
  8. 8
    ДругоеThe 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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08968708B2uspto-grants-2015_03