HRID1195333

反应详情

EQUATION

反应方程式

HRID 1195333 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 chilled (0° C.) solution of ethyl 3,3-bis(4-fluorophenyl)-2-[1-(1-methylethyl)-1H-tetrazol-5-yl]-2-propenoate (0.95 g, 2.39 mmoles) in 20 mL of 1:1 (v/v) mixture of tetrahydrofuran and methanol was added an aqueous solution of LiOH (4.0 mL, 3 Molar) in one single portion. The reaction mixture was stirred at 0° C. for 15 minutes followed by warming up to ambient temperature. Saponification was allowed to proceed at room temperature for four hours forming a very pale clear solution. The crude reaction mixture was diluted with 12 mL of 2M H2SO4 and the product was extracted into diethyl ether (40 mL×2). The organic layers were combined, dried over MgSO4, concentrated under reduced pressure and then vigorously dried under high vacuum (0.01 mmHg) at room temperature for 24 hours to yield the title compound. The propenoic acid was then utilized in the next step without further purification.

WORKUP

后处理

  1. temperatureby warming up to ambient temperature
  2. waitto proceed at room temperature for four hours
  3. customforming a very pale clear solution
  4. customThe crude reaction mixture
  5. extractionthe product was extracted into diethyl ether (40 mL×2)
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated under reduced pressure
  8. customvigorously dried under high vacuum (0.01 mmHg) at room temperature for 24 hours