HRID54547

反应详情

EQUATION

反应方程式

HRID 54547 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 4-(2-hydroxyethyl)piperidine (21.5 g), 4-fluorobenzaldehyde (17.5 ml) and p-toluene sulfonic acid (3 mg) in benzene (200 ml) was refluxed with separating water as the benzene azeotrope. After 2 hours, the mixture was evaporated in vacuo. The residue was dissolved in methanol (200 ml) and sodium borohydride (6.3 g) was added thereto at 5° C. After stirring at ambient temperature for 1 hour, the mixture was evaporated in vacuo. 4N Hydrochloric acid (200 ml) was added to the residue and washed with ethyl acetate. The aqueous layer was made basic to pH 10 with potassium carbonate and extracted with ethyl acetate. The extract was washed with water and brine, and dried over magnesium sulfate, and evaporated in vacuo to give 1-(4-fluorobenzyl)-4-(2-hydroxyethyl)piperidine (32.0 g) as an oil.

WORKUP

后处理

  1. customthe mixture was evaporated in vacuo
  2. dissolutionThe residue was dissolved in methanol (200 ml)
  3. additionsodium borohydride (6.3 g) was added
  4. customat 5° C
  5. customthe mixture was evaporated in vacuo
  6. addition4N Hydrochloric acid (200 ml) was added to the residue
  7. washwashed with ethyl acetate
  8. extractionextracted with ethyl acetate
  9. washThe extract was washed with water and brine
  10. dry with materialdried over magnesium sulfate
  11. customevaporated in vacuo