Реакция #670119

ord-ec134a99aff2424b97fdae11e0834191

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеa reaction scheme
  2. 2
    Другоеa compound that is useful as a precursor in the preparation of Group I compounds
  3. 3
    workup.STIRRINGThe reaction mixture is stirred overnight at room temperature
  4. 4
    Другоеacetone is removed under vacuum
  5. 5
    workup.DISSOLUTIONThe residue is dissolved in water (10 ml)

Методика

FIG. 2A illustrates a reaction scheme for preparing 2-(4-aminophenoxy)-2-methyl propionic acid, a compound that is useful as a precursor in the preparation of Group I compounds. In accordance with the scheme of FIG. 2A, 8 grams (g) (0.2 mol) of pulverized sodium hydroxide is added to a suspension of 5.28 g (0.035 mol) of p-acetamidophenol in 23 ml (0.4 mol) of acetone. The reaction mixture is stirred at room temperature for 1/2 hour. Subsequently, 3.58 g (0.03 mol) of chloroform is added dropwise over the course of 30 minutes. The reaction mixture is stirred overnight at room temperature and acetone is removed under vacuum. The residue is dissolved in water (10 ml), followed by acidification with 37% hydrochloric acid (HCl) to produce a pale yellow precipitate of 2-(4-acetaminophenoxy)-2-methyl propionic acid (5 g, 60% yield), crystallized from methanol, mp 69-71° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05927283uspto-grants-1999_07