反应 #45798

ord-817f578aa2bd495588519a1bd2cabb1e

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他the insoluble matter was removed by filtration (with washing with acetonitrile (400 ml))
  2. 2
    浓缩The filtrate was concentrated under reduced pressure (about 800 ml of acetonitrile
  3. 3
    其他was evaporated away), and water (800 ml)
  4. 4
    workup.ADDITIONwas added to the residue
  5. 5
    洗涤The precipitated crystal was washed with water
  6. 6
    其他dried

实验过程

5-Bromo-4-fluoro-2-hydroxy-3-nitrobenzoic acid (I-228) (35.89 g, 0.128 mol) was dissolved in acetonitrile (600 ml), then at room temperature, potassium carbonate (53.1 g, 0.358 mol) was added, and dimethyl sulfate (30.3 ml, 0.32 mol was dropwise added. After staring at 60° C. for 2.5 hour and then cooling to room temperature, the insoluble matter was removed by filtration (with washing with acetonitrile (400 ml)). The filtrate was concentrated under reduced pressure (about 800 ml of acetonitrile was evaporated away), and water (800 ml) was added to the residue, followed by stirring at room temperature. The precipitated crystal was washed with water and dried to obtain the entitled compound (36.5 g, 92%) as a pale yellow solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07737166B2uspto-grants-2010_06