反応 #1769

ord-48df0370b6c1448ea65c1fd6355a24c2

反応方程式

COC(=O)c1ccc(O)cc1OC
methyl 4-hydroxy-2-methoxybenzoate
F[n+]1cc(Cl)cc(Cl)c1.O=S(=O)([O-])C(F)(F)F
3,5-dichloro-1-fluoropyridinium triflate
COC(=O)c1cc(F)c(O)cc1OC
methyl 5-fluoro-4-hydroxy-2-methoxybenzoate

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The solution was refluxed for 48 h
  2. 2
    その他The crude oil was purified by pressurized silica gel column chromatography
  3. 3
    その他Evaporation of the CH2Cl2

実験手順

To a stirred solution of the methyl 4-hydroxy-2-methoxybenzoate (1 g, 5 mmol, from Step 3) in CH2Cl2 (20 mL) was added 3,5-dichloro-1-fluoropyridinium triflate (2.25 g, 6 mmol). The solution was refluxed for 48 h and then cooled to ambient temperature and stripped down under reduced pressure. The crude oil was purified by pressurized silica gel column chromatography using 99:1 CH2Cl2 :MeOH. Evaporation of the CH2Cl2 :MeOH mixture gave the desired methyl 5-fluoro-4-hydroxy-2-methoxybenzoate as a white powder.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05726172uspto-grants-1998_03