反应 #1605771

ord-2248bc55a7674b14921a08ad02a489ba

反应方程式

Cc1ccc(C(=O)O)c(O)c1
2-hydroxy-4-methylbenzoic acid
O=C([O-])[O-].[K+].[K+]
K2CO3
[K+].[OH-]
KOH
Cl
HCl
COc1cc(C)ccc1C(=O)O
2-methoxy-4-methylbenzoic acid

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度the reaction mixture heated
  2. 2
    温度at reflux for 48 hrs
  3. 3
    过滤was filtered
  4. 4
    其他the filtrate was evaporated
  5. 5
    其他to give the crude methyl 2-methoxy-4-methylbenzoate
  6. 6
    温度the solution heated
  7. 7
    温度at reflux 48 hrs
  8. 8
    温度After cooling the reaction mixture
  9. 9
    萃取extracted with ethyl acteate
  10. 10
    洗涤The organic layer was washed with brine
  11. 11
    干燥dried over MgSO4
  12. 12
    过滤filtered
  13. 13
    其他evaporated
  14. 14
    其他The residue was triturated with Ethyl acetate/Hexane

实验过程

To a solution of 2-hydroxy-4-methylbenzoic acid (25 g, 0.164 mol) in acetone (350 mL) was added K2CO3 (68 g, 0.492 mmol) followed by MeI (41 mL, 0.656 mmol) and the reaction mixture heated at reflux for 48 hrs. After cooling to r.t. the reaction mixture was filtered and the filtrate was evaporated to give the crude methyl 2-methoxy-4-methylbenzoate. KOH (11.3 g, 1.2 eq) was dissolved in MeOH (300 mL) and the crude ester was added to the mixture and the solution heated at reflux 48 hrs. After cooling the reaction mixture was acidified with aq. HCl (1N) and extracted with ethyl acteate. The organic layer was washed with brine, dried over MgSO4, filtered and evaporated. The residue was triturated with Ethyl acetate/Hexane to give 20 g of 2-methoxy-4-methylbenzoic acid as a cream white solid (85% yield)

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09072313B2uspto-grants-2015_07