反应 #1596973

ord-9f45caefc9094fa28cf0559b401885ee

反应方程式

O=C(O)c1ccc(O)cc1
p-hydroxybenzoic acid
C=CCCCCCCBr
8-bromo-1-octene
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(=O)N(C)C
N,N-dimethylacetamide
C=CCCCCCCOc1ccc(C(=O)O)cc1
4-(7-octenyloxy)-benzoic acid

溶剂

反应条件

温度
120°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度After cooled
  2. 2
    萃取extracted with ethyl acetate (500 mL)
  3. 3
    洗涤washed two times with water (100 mL)
  4. 4
    干燥This was dried with anhydrous magnesium sulfate
  5. 5
    过滤filtered
  6. 6
    其他The solvent was removed through concentration under reduced pressure
  7. 7
    workup.DISSOLUTIONthe residue was dissolved in methanol (100 mL)
  8. 8
    workup.ADDITIONgradually added
  9. 9
    温度heated
  10. 10
    温度under reflux for 2 hours
  11. 11
    温度After cooled
  12. 12
    过滤the formed crystal was collected through filtration
  13. 13
    洗涤washed with water
  14. 14
    其他This was dried
  15. 15
    其他to give TP-5C (63.3 g, 85%)

实验过程

p-hydroxybenzoic acid (33.2 g), 8-bromo-1-octene (57.3 g), potassium carbonate (41.5 g) and N,N-dimethylacetamide (200 mL) were put into a 500-mL three-neck flask, and stirred at 120° C. for 5 hours. After cooled, the reaction mixture was poured into water (200 mL), extracted with ethyl acetate (500 mL), and washed two times with water (100 mL). This was dried with anhydrous magnesium sulfate and then filtered. The solvent was removed through concentration under reduced pressure, the residue was dissolved in methanol (100 mL), and a methanol solution (20 mL) of potassium hydroxide (16.8 g) was dropwise and gradually added thereto, and heated under reflux for 2 hours. After cooled, the formed crystal was collected through filtration and washed with water. This was dried to give TP-5C (63.3 g, 85%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08211598B2uspto-grants-2012_07