HRID750550

反应详情

EQUATION

反应方程式

HRID 750550 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

10.0 g (0.042 mol) of methyl 9-xanthenecarboxylate (obtainable according to step 1.1.a) are dissolved in 100 mL of tetrahydrofuran and combined batchwise with 5.16 g (0.044 mol) of potassium tert-butoxide while cooling. Then at about 18° C. to 22° C., 6.296 mL (0.083 mol) of bromoethane are added dropwise; after it has all been added, the mixture is stirred for about 1.5 hours at ambient temperature. The precipitate formed is suction filtered and the solvent is removed by distillation. The residue remaining is taken up in diethyl ether and extracted with water. The organic phase is dried over magnesium sulfate and the solvent is removed by distillation. The crude product obtained is used in the next step without any further purification. Yield: 7.92 g of yellow oil (70% of theoretical yield).

WORKUP

后处理

  1. temperaturewhile cooling
  2. additionall been added
  3. customThe precipitate formed
  4. filtrationfiltered
  5. customthe solvent is removed by distillation
  6. extractionextracted with water
  7. dry with materialThe organic phase is dried over magnesium sulfate
  8. customthe solvent is removed by distillation