반응 #51654

ord-c99ce4ac2a264f8288ccd8735e8672e3

반응 방정식

OB(O)c1ccc(F)cc1
4-fluorophenyl boronic acid
COC(=O)c1ccc(O)cc1
methyl 4-hydroxybenzoate
O=C(O)c1ccc(Oc2ccc(F)cc2)cc1
4-(4-fluorophenoxy)benzoic acid
수율 91.9%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타bubbling through it
  2. 2
    workup.ADDITIONThe reaction mixture is diluted with CH2Cl2
  3. 3
    여과filtered through silica gel
  4. 4
    세척The silica gel is washed with EtOAc-heptane
  5. 5
    농축The solution is concentrated in vacuo
  6. 6
    workup.DISSOLUTIONdissolved in dioxane (15 mL)
  7. 7
    workup.ADDITIONTo this solution is added aqueous LiOH (1N, 15 mL)
  8. 8
    workup.STIRRINGstirred for 18 hours at room temperature
  9. 9
    workup.ADDITIONTo this reaction mixture is added aqueous HCl (1N) until acidic,
  10. 10
    여과The resulting precipitate is collected by filtration
  11. 11
    세척rinsed with water
  12. 12
    기타dried in vacuo

실험 절차

To a flask with 4-fluorophenyl boronic acid (2.1 g, 15 mmol), copper(II) acetate (1.4 g, 7.5 mmol), activated powdered molecular sieves (approximately 2 g), and methyl 4-hydroxybenzoate (1.2 g, 7.5 mmol) is added TEA (5.2 mL, 38 mmol) followed by CH2Cl2 (75 mL). The reaction is stirred for 16 hours at room temperature with air bubbling through it. The reaction mixture is diluted with CH2Cl2 and filtered through silica gel. The silica gel is washed with EtOAc-heptane. The solution is concentrated in vacuo and dissolved in dioxane (15 mL). To this solution is added aqueous LiOH (1N, 15 mL) and stirred for 18 hours at room temperature. To this reaction mixture is added aqueous HCl (1N) until acidic, having a pH less than 6. The resulting precipitate is collected by filtration and rinsed with water, and dried in vacuo to give 4-(4-fluorophenoxy)benzoic acid (1.6 g, 90%). MS for C13H9FO3 (ESI) (M−H)− m/z 231.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06852716B2uspto-grants-2005_02