HRID850428

反应详情

EQUATION

反应方程式

HRID 850428 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

3-Methoxy-2-pentyloxybenzoic acid (1.5 g, 6.3 mmol), methanol (10 ml) and conc. sulfuric acid (1 drop) were mixed, and this solution was refluxed under heating for 7 hours. Methanol was evaporated under reduced pressure, and a saturated aqueous sodium hydrogencarbonate solution (3 ml) was added. The aqueous layer was extracted twice with ethyl acetate (20 ml). The organic layers were combined, washed twice with a saturated aqueous sodium hydrogencarbonate solution (5 ml) and once with saturated brine (5 ml), and dried over anhydrous magnesium sulfate. The drying agent was filtered off, and the filtrate was concentrated under reduced pressure. THF (15 ml) was added to the obtained residue in a stream of argon, and the mixture was cooled to 0° C. Lithium aluminum hydride (0.49 g, 13 mmol) was added to this solution, and the mixture was stirred for 1 hour. Water (0.4 ml), a 1N aqueous sodium hydroxide solution (0.4 ml) and water (1.2 ml) were successively added dropwise to the reaction mixture. Ether (60 ml) was added, and the mixture was vigorously stirred for 1 hour. The inorganic salt was filtered off, and the filtrate was concentrated under reduced pressure to give a crude product of (3-methoxy-2-pentyloxyphenyl)methanol. The product was not further purified, and used in the next reaction.

WORKUP

后处理

  1. temperaturethis solution was refluxed
  2. temperatureunder heating for 7 hours
  3. customMethanol was evaporated under reduced pressure
  4. additiona saturated aqueous sodium hydrogencarbonate solution (3 ml) was added
  5. extractionThe aqueous layer was extracted twice with ethyl acetate (20 ml)
  6. washwashed twice with a saturated aqueous sodium hydrogencarbonate solution (5 ml) and once with saturated brine (5 ml)
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationThe drying agent was filtered off
  9. concentrationthe filtrate was concentrated under reduced pressure
  10. additionTHF (15 ml) was added to the obtained residue in a stream of argon
  11. stirringthe mixture was vigorously stirred for 1 hour
  12. filtrationThe inorganic salt was filtered off
  13. concentrationthe filtrate was concentrated under reduced pressure