HRID1656481

反应详情

EQUATION

反应方程式

HRID 1656481 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

In a 1 liter 4-necked round-bottomed flask were placed 500 ml of methylene chloride and cooled down to -78° C. 41.3 g (0.33 mole) of oxalyl chloride were added slowly, followed by dropwise addition of 56.4 g (0.72 mole) of dry dimethylsulfoxide in 30 ml of methylene chloride, all the while keeping the temperature below -70° C. After the addition was completed the reaction mixture was stirred at -78° C. for 30 minutes and 60 g (0.36 mole) of the previously prepared 3-hydroxymethyl-5-methylbenzoic acid were added in 1 portion, followed by dropwise addition of 131.4 g (1.3 mole) of triethylamine, keeping the temperature below -65° C. during each of the additions. The reaction mixture was then warmed up slowly to room temperature, stirred for 90 minutes and then washed with 2% aqueous sodium hydroxide (3×500 ml). The combined basic layers were washed with hexane once and acidified with concentrated hydrochloric acid and then extracted with ethyl acetate (4×500 ml). The combined organic layers were washed with water (1×500 ml) and then with brine (1×300 ml) and dried over anhydrous magnesium sulfate. The solvent was then eliminated in a rotavap. The resulting oily product was triturated with hexane and filtered yielding 52 g (88%) 3-formyl-5-methylbenzoic acid as a tan solid.

WORKUP

后处理

  1. customIn a 1 liter 4-necked round-bottomed flask were placed
  2. customthe temperature below -70° C
  3. additionAfter the addition
  4. customthe temperature below -65° C.
  5. temperatureThe reaction mixture was then warmed up slowly to room temperature
  6. stirringstirred for 90 minutes
  7. washwashed with 2% aqueous sodium hydroxide (3×500 ml)
  8. washThe combined basic layers were washed with hexane once
  9. extractionextracted with ethyl acetate (4×500 ml)
  10. washThe combined organic layers were washed with water (1×500 ml)
  11. dry with materialwith brine (1×300 ml) and dried over anhydrous magnesium sulfate
  12. customThe solvent was then eliminated in a rotavap
  13. customThe resulting oily product was triturated with hexane
  14. filtrationfiltered