HRID1034415

反应详情

EQUATION

反应方程式

HRID 1034415 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Benzoyl chloride (13.3 mL, 0.115 mole) was added dropwise over 0.5 hour to a 0° C. solution of 4-piperidineethanol (14.8 g, 0.115 mole) and dry triethylamine (18 mL, 0.13 mole) in dichloromethane with mechanical stirring. After 16 hours at room temperature, the mixture was quenched with 1.0 M aqueous NaOH (150 mL), then extracted with ethyl acetate (1 L). The organic phase was extracted further with H2O (125 mL), then brine (125 mL), dried (MgSO4), filtered, and concentrated in vacuo. The crude product was purified by chromatography on silica gel, eluting with chloroform to 6% methanol in chloroform, followed by concentration in vacuo and drying at 100° C. under high vacuum for 1.5 hour to yield a viscous oil (25.1 g, 94%). IR (neat): 3409 cm-1 (s,br), 1613(s). HRMS: Calculated for C14H19NO2 : 233.1416; found: 233.1410.

WORKUP

后处理

  1. customthe mixture was quenched with 1.0 M aqueous NaOH (150 mL)
  2. extractionextracted with ethyl acetate (1 L)
  3. extractionThe organic phase was extracted further with H2O (125 mL)
  4. dry with materialbrine (125 mL), dried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe crude product was purified by chromatography on silica gel
  8. washeluting with chloroform to 6% methanol in chloroform
  9. concentrationfollowed by concentration in vacuo
  10. customdrying at 100° C. under high vacuum for 1.5 hour