HRID2250885

反应详情

EQUATION

反应方程式

HRID 2250885 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of (2-bromo-4-fluoro-phenoxy)-acetic acid-t-butyl ester (5.1 g, 16.71 mmol) in DME (60 ml)/2M Na2CO3 (29.25 ml, 58.50 mmol) was treated with 2-trifluoromethoxyphenylboronic acid (5.16 g, 25.08 mmol), and Pd[PPh3]4 (3.87 g, 3.33 mmol) in a microwave oven at 150° C. for 15 min. The reaction mixture was partitioned between 1N HCl and ethyl acetate. The organic layer was successively washed with 1N NaOH and brine, then dried over sodium sulfate, filtered, and concentrated. The crude was absorbed on silica and purified on a silica gel column with a 8-10% ethyl acetate/hexanes gradient to afford 4.65 g of colorless oil (t-butyl ester). This material was dissolved in 4N HCl/dioxane (40 ml) and stirred at 60° C. for 2 h and then at rt overnight. Concentration under reduced pressure afforded the product as colorless oil (4.17 g, 24%).

WORKUP

后处理

  1. customThe reaction mixture was partitioned between 1N HCl and ethyl acetate
  2. washThe organic layer was successively washed with 1N NaOH and brine
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude was absorbed on silica
  7. custompurified on a silica gel column with a 8-10% ethyl acetate/hexanes gradient