HRID28754

反应详情

EQUATION

反应方程式

HRID 28754 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
55 °C

PROCEDURE

实验过程

A solution of 5-(2-benzyloxy-ethyl)-2-hydroxy-cyclohexanecarboxylic acid methyl ester (Intermediate R2, 0.72 g, 2.48 mmol) in pyridine (10 mL) was treated with SOCl2 (0.73 mL, 12.4 mmol) at −20° C. The mixture was allowed to react for 15 m and was then warmed to 55° C. for 16 h. The solvents were removed under vacuum and the residue was diluted in ether at 0° C. The solution was quenched with water, washed with 1M HCl, 5% NaOH and brine. The organic material was dried over MgSO4 filtered and freed of solvent. The mixture was diluted with benzene and water was removed by azeotropic distillation under vacuum. The residue was dissolved in benzene (15 mL) and DBU (0.76 mL, 5 mmol) was added. The mixture was reacted for 30 m at rt. After work-up and chromatography on SiO2 with 20% EtOAc:Hx 5-(2-benzyloxy-ethyl)-cyclohex-1-enecarboxylic acid methyl ester (Intermediate R3) was isolated 0.56 g (82%).

WORKUP

后处理

  1. customto react for 15 m
  2. customThe solvents were removed under vacuum
  3. additionthe residue was diluted in ether at 0° C
  4. customThe solution was quenched with water
  5. washwashed with 1M HCl, 5% NaOH and brine
  6. dry with materialThe organic material was dried over MgSO4
  7. filtrationfiltered
  8. additionThe mixture was diluted with benzene and water
  9. customwas removed by azeotropic distillation under vacuum
  10. dissolutionThe residue was dissolved in benzene (15 mL)
  11. customThe mixture was reacted for 30 m at rt