HRID1833932

反应详情

EQUATION

反应方程式

HRID 1833932 的结构方程式

PROCEDURE

实验过程

A mixture of 4-(methylsulfonyl)-m-cresol (18.6 g., 0.1 mole), epichlorohydrin (60 g., 0.65 mole) and 0.6 g. of pyrrolidine is heated on steam bath for 12 hr. Excess epichlorohydrin is removed under reduced pressure, the resulting chlorohydrin derivative taken up in 50 ml. of absolute ethanol and filtered through diatomaceous earth. Isopropylamine (50 g., 0.85 mole) and 0.1 g. of potassium iodide are added to the ethanol filtrate of the epichlorohydrin derivative and the mixture is refluxed for 18 hr. and filtered. Concentration of the filtrate under reduced pressure affords a residue which is taken up in 70 ml. of 1N hydrochloric acid and 300 ml. of absolute ethanol. Distillables are removed under reduced pressure and the resulting residue stirred with ether to provide solid crude product. Crystallization of the crude product from butanone-methanol and again from 95% ethanol-ether, affords 1-(ISOPROPYLAMINO)-3-[4-(METHYLSULFONYL)-m-TOLYLOXY]-2-PROPANOL HYDROCHLORIDE, m.p. 177.0°-179.0° C. (corr.) in a 62% overall yield. A sample, m.p. 176.0°-178.0° C. (corr), analyzed as follows.

WORKUP

后处理

  1. customExcess epichlorohydrin is removed under reduced pressure
  2. filtrationof absolute ethanol and filtered through diatomaceous earth
  3. temperaturethe mixture is refluxed for 18 hr
  4. filtrationand filtered
  5. customConcentration of the filtrate under reduced pressure affords a residue which
  6. customDistillables are removed under reduced pressure
  7. customto provide solid crude product
  8. customCrystallization of the crude product from butanone-methanol