HRID1431621

反应详情

EQUATION

反应方程式

HRID 1431621 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

The (2-bromo-4-fluorophenyl)(methyl)sulfane (700 mg, 3.17 mmol) was dissolved in THF (5 mL) and cooled to −78° C. To the cooled solution was added n-BuLi (2.18 mL, 3.48 mmol) dropwise. The reaction was stirred for 2 min at −78° C. then the triisopropyl borate (0.804 mL, 3.48 mmol) was added dropwise and the reaction mixture was allowed to warm to 0° C. over a period of approximately 90 min. The reaction was quenched by addition of 1N HCl solution and was stirred for 5 min. The mixture was then extracted with EtOAc (2×50 mL). The combined organic layers were washed with water (1×30 mL), brine (1×30 mL) and dried over magnesium sulfate. The crude product was then triturated with hexanes. The resulting solid was purified by medium pressure chromatography (silica gel, 0 to 50% EtOAc:hexanes) to give 5-fluoro-2-(methylthio)phenylboronic acid. Mass Spectrum (ESI) m/e=187.0 (M+1).

WORKUP

后处理

  1. temperatureto warm to 0° C. over a period of approximately 90 min
  2. customThe reaction was quenched by addition of 1N HCl solution
  3. stirringwas stirred for 5 min
  4. extractionThe mixture was then extracted with EtOAc (2×50 mL)
  5. washThe combined organic layers were washed with water (1×30 mL), brine (1×30 mL)
  6. dry with materialdried over magnesium sulfate
  7. customThe crude product was then triturated with hexanes
  8. customThe resulting solid was purified by medium pressure chromatography (silica gel, 0 to 50% EtOAc:hexanes)