تفاعل #46447

ord-181d57e23e8f4d86b4e5d685e0a7fe14

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas removed by distillation at 80° C
  2. 2
    workup.ADDITIONAdditional benzene (50 ml) was added to the reaction
  3. 3
    درجة الحرارةAfter heating
  4. 4
    درجة الحرارةat reflux for 3 hours
  5. 5
    درجة الحرارةto cool to room temperature
  6. 6
    أخرىthe organic layer was separated
  7. 7
    غسيلwashed with H2O
  8. 8
    تجفيفAfter drying over MgSO4
  9. 9
    أخرىthe solvent was removed under reduced pressure
  10. 10
    أخرىThe resulting residue was purified by flash chromatography

الإجراء التجريبي

To a solution of 3-fluorophenol (1 ml, 11 mmol) in THF (20 ml) in a three-neck flask was added ethylmagnesium bromide (5.5 ml, 5.5 mmol, 1M in THF). After stirring at room temperature for 2 hours, benzene was added to the reaction mixture and THF was removed by distillation at 80° C. Additional benzene (50 ml) was added to the reaction, followed by NEt3 (2.3 ml, 16.5 mmol) and paraformaldehyde (1 g, 33.3 mmol). After heating at reflux for 3 hours, the reaction mixture was allowed to cool to room temperature and was poured into 250 ml of 10% HCl. EtOAc was added and the organic layer was separated and washed with H2O. After drying over MgSO4, the solvent was removed under reduced pressure. The resulting residue was purified by flash chromatography to give 4-fluoro-2-hydroxy-benzaldehyde as a white solid (560 mg, 36%), 1H NMR (CDCl3, 300 MHz) δ: 6.71 (m, 2H), 7.56 (dd, 1H, J=6.3 Hz, 8.6 Hz), 9.84 (s, 1H), 11.36 (s, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07741326B2uspto-grants-2010_06