تفاعل #1769

ord-48df0370b6c1448ea65c1fd6355a24c2

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe solution was refluxed for 48 h
  2. 2
    أخرىThe crude oil was purified by pressurized silica gel column chromatography
  3. 3
    أخرىEvaporation of the CH2Cl2

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726172uspto-grants-1998_03