HRID418055

反应详情

EQUATION

反应方程式

HRID 418055 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a solution of 2,3-dimethylphenol (25 g, 204 mmol) in DMSO (205 mL) was added 4-bromo-butyric acid ethyl ester (40.96 g, 210 mmol) and lithium hydride (2.0 g, 250 mmol) at room temperature. The resulting light brown solution was stirred for 2 days. Then, the reaction mixture was cooled to 0° C. and water (200 mL) was added slowly. The organic compound was extracted into hexanes (2×200 mL). The combined organic extracts were washed with brine solution (150 mL) and the organic solution was dried over anhydrous magnesium sulfate. Filtration of the drying agent and the removal of the solvent gave light brown oil. The crude mixture was purified by using a Biotage™ (40 L) column chromatography eluting with 5% ethyl acetate in hexanes to isolate 4-(2,3-dimethyl-phenoxy)-butyric acid ethyl ester (45.32 g, 94%) as a colorless oil: ES(+)-HRMS m/e calculated for C14H20O3 (M+)+ 236.1412, found 236.1419.

WORKUP

后处理

  1. extractionThe organic compound was extracted into hexanes (2×200 mL)
  2. washThe combined organic extracts were washed with brine solution (150 mL)
  3. dry with materialthe organic solution was dried over anhydrous magnesium sulfate
  4. filtrationFiltration of the drying agent
  5. customthe removal of the solvent
  6. customgave light brown oil
  7. customThe crude mixture was purified
  8. washeluting with 5% ethyl acetate in hexanes