HRID572545

反应详情

EQUATION

反应方程式

HRID 572545 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

A mixture of methyl 4-bromo-3-methylbenzoate (20 g, 87 mmol), 2-(trifluoromethyl)benzeneboronic acid (24.9 g, 131 mmol), potassium carbonate (24 g, 175 mmol) and bis(tricyclohexylphosphine)palladium (II) dichloride (65 mg, 0.1 mmol) was prepared in dioxane (200 mL) and water (50 mL) under N2 atmosphere. The mixture was heated at 100° C. for 3 hours. A 5N aqueous solution of NaOH (100 mL) was added and the reaction mixture was stirred at 100° C. for one additional hour. The reaction mixture was cooled at RT and the aqueous layer was removed. The organic layer was filtered through a celite pad, concentrated until 75 mL under reduced pressure, diluted with water (125 mL) and washed with MTBE (2×200 mL). The aqueous layer was acidified to pH 1 with a 5N aqueous solution of HCl (25 mL) and extracted with MTBE (2×100 mL). The organic layers were combined, dried (Na2SO4) and filtered through a celite pad. The solution was concentrated until 100 mL, then heptane was added (200 mL). The mixture was concentrated until 100 mL. The precipitate was filtered off and rinsed twice with heptane, then dried under reduced pressure to give the title compound as a white powder (22.5 g, 92%). HPLC (Method A), Rt 4.4 min (purity: 100%). LC/MS (Method B): 279.0 (M−H)−. 1H NMR (DMSO-d6, 300 MHz) δ 13.0 (s, 1H), 7.87 (m, 2H), 7.80 (dd, J=7.9, 1.6 Hz, 1H), 7.75 (m, 1H), 7.64 (m, 1H), 7.34 (d, J=7.6 Hz, 1H), 7.23 (d, J=7.9 Hz, 1H), 2.02 (s, 3H).

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled at RT
  2. customthe aqueous layer was removed
  3. filtrationThe organic layer was filtered through a celite pad
  4. concentrationconcentrated until 75 mL under reduced pressure
  5. additiondiluted with water (125 mL)
  6. washwashed with MTBE (2×200 mL)
  7. extractionextracted with MTBE (2×100 mL)
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered through a celite pad
  10. concentrationThe solution was concentrated until 100 mL
  11. additionheptane was added (200 mL)
  12. concentrationThe mixture was concentrated until 100 mL
  13. filtrationThe precipitate was filtered off
  14. washrinsed twice with heptane
  15. customdried under reduced pressure