반응 #513491

ord-a00f3bf499d34775ab76d5f2267bb0c4

반응 방정식

COC(=O)Cc1cc(OS(=O)(=O)C(F)(F)F)cc(OS(=O)(=O)C(F)(F)F)c1
(3,5-bis-trifluoromethanesulfonyloxy-phenyl)-acetic acid methyl ester
OB(O)c1ccc(Cl)cc1
4-chlorophenyl boronic acid
O=C([O-])[O-].[K+].[K+]
K2CO3
COC(=O)Cc1cc(-c2ccc(Cl)cc2)cc(-c2ccc(Cl)cc2)c1
(4,4″-Dichloro-[1,1′;3′,1″]terphenyl-5′-yl)-acetic acid methyl ester

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과filtered
  2. 2
    workup.ADDITIONdiluted with EtOAc
  3. 3
    세척washed with Na2CO3, dil HCl, brine
  4. 4
    건조dried (MgSO4)
  5. 5
    기타evaporated under reduced pressure
  6. 6
    기타to give an off white solid
  7. 7
    기타The residue was purified by flash column chromatography (EtOAc:petroleum ether), 1H NMR (CDCl3) δ 7.61 (t, 1H), 7.55 (d, 4H), 7.46 (d, 2H), 7.42 (d, 4H), 3.75 (s, 2H), 3.73 (s, 3H)

실험 절차

A solution of (3,5-bis-trifluoromethanesulfonyloxy-phenyl)-acetic acid methyl ester (250 mg, 0.56 mmol), 4-chlorophenyl boronic acid (219 mg, 1.4 mmol), K2CO3 (2 M solution in H2O, 1.1 mL, 2.24 mmol) in DME (4.0 mL) and heated to 80° C. in the presence of bis(tri-t-butylphosphine) palladium (0) (cat) for 4 hrs. The mixture was cooled to room temperature filtered, diluted with EtOAc, washed with Na2CO3, dil HCl, brine, dried (MgSO4) and evaporated under reduced pressure to give an off white solid. The residue was purified by flash column chromatography (EtOAc:petroleum ether), 1H NMR (CDCl3) δ 7.61 (t, 1H), 7.55 (d, 4H), 7.46 (d, 2H), 7.42 (d, 4H), 3.75 (s, 2H), 3.73 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08106236B2uspto-grants-2012_01