HRID464986

反应详情

EQUATION

反应方程式

HRID 464986 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 8.50 g (28.3 mole) of 5-oxo-1-(phenylmethyl)-N-(2,2,2-trifluoroethyl)-3-pyrrolidinecarboxamide in 100 ml tetrahydrofuran was added dropwise to 3.22 g (84.9 mmole) of lithium aluminum hydride in 50 ml tetrahydrofuran. The reaction was refluxed two hours, then stirred at room temperature overnight. The reaction was cooled in an ice bath and 3.2 ml of water, 3.2 ml of 15% sodium hydroxide, and 9.6 ml of water were added. The precipitated salts were filtered and washed with hot ethanol. The combined filtrates were concentrated under reduced pressure. The residue was taken up in dichloromethane, filtered, and dried over magnesium sulfate. The solvent was removed at reduced pressure to give 7.15 g of 1-(phenylmethyl)-N-(2,2,2-trifluoroethyl)-3-pyrrolidinemethanamine.

WORKUP

后处理

  1. temperatureThe reaction was refluxed two hours
  2. temperatureThe reaction was cooled in an ice bath
  3. filtrationThe precipitated salts were filtered
  4. washwashed with hot ethanol
  5. concentrationThe combined filtrates were concentrated under reduced pressure
  6. filtrationfiltered
  7. dry with materialdried over magnesium sulfate
  8. customThe solvent was removed at reduced pressure