HRID597648

反应详情

EQUATION

反应方程式

HRID 597648 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

7.5 g (0.03 mol) of 1-[p-(2-methoxycarbonylaminovinyl)-phenoxy]-2,3-epoxypropane are dissolved in 75 ml of acetonitrile and added dropwise to a boiling stirred solution of 3.34 g (0.029 mol) of β-aminobutyric acid amide in 75 ml of aceto-nitrile. The mixture is stirred for 20 hours under reflux, the solvent is removed by distillation under reduced pressure and the oil which remains is partitioned between 350 ml of 0.1 N hydrochloric acid and 300 ml of ethyl acetate. The hydrochloric acid extract is separated off, rendered alkaline with sodium carbonate and extracted four times with 100 ml of ethyl acetate at a time. The organic phases are dried over sodium sulphate and evaporated under reduced pressure. The resulting oil yields 1-[p-(2-methoxycarbonylaminovinyl)-phenoxy]-2-hydroxy-3-(2-carbamoyl-1-methyl-ethylamino)-propane, of melting point 109°-111°C, from acetone acetate.

WORKUP

后处理

  1. additionadded dropwise to a boiling
  2. temperatureunder reflux
  3. customthe solvent is removed by distillation under reduced pressure
  4. customthe oil which remains is partitioned between 350 ml of 0.1 N hydrochloric acid and 300 ml of ethyl acetate
  5. extractionThe hydrochloric acid extract
  6. customis separated off
  7. extractionextracted four times with 100 ml of ethyl acetate at a time
  8. dry with materialThe organic phases are dried over sodium sulphate
  9. customevaporated under reduced pressure