HRID1052896

反应详情

EQUATION

反应方程式

HRID 1052896 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

10 gms of 3-[5-Benzyloxy-2-[(4-benzyloxy-phenyl)-(4-fluoro-phenylamino)-methyl]-5-(4-fluoro-phenyl)-pentanoyl]-4-phenyl-oxazolidin-2-one was taken in dichloromethane, to this 3.6 gms of sodium methoxide was added followed by 3.2 ml of dimethylcarbonate, and 500 ml of dichloromethane. Reaction mass was stirred for about 5-7 hours. To the reaction mass 0.1 ml of hydrochloric acid was added. Separated the layers and extract the aqueous layer with 25 ml of methylene dichloride. The organic layer was washed with water and dried over sodium sulphate. Distilled the solvent completely under reduced pressure at 50-55° C. and 85 ml of methanol was added. Stirred the reaction mass for about 1-2 hours, filtered and washed with methanol and dried at 50-55° C. to get 5 gms of 5-Benzyloxy-2-[(4-benzyloxy-phenyl)-(4-fluoro-phenylamino)-methyl]-5-(4-fluoro-phenyl)-pentanoic acid methyl ester.

WORKUP

后处理

  1. additionwas added
  2. customReaction mass
  3. customSeparated the layers
  4. extractionextract the aqueous layer with 25 ml of methylene dichloride
  5. washThe organic layer was washed with water
  6. dry with materialdried over sodium sulphate
  7. distillationDistilled the solvent completely under reduced pressure at 50-55° C.
  8. addition85 ml of methanol was added
  9. stirringStirred the reaction mass for about 1-2 hours
  10. filtrationfiltered
  11. washwashed with methanol
  12. customdried at 50-55° C.