Réaction #6535

ord-2356c1ff19bd4e029e4fdd495659ed04

Équation de réaction

CC(C)(Oc1ccc(N)cc1)C(=O)O
2-(4-aminophenoxy)-2-methyl propionic acid
ClC(Cl)Cl
chloroform
[Na+].[OH-]
sodium hydroxide
CC(=O)Nc1ccc(O)cc1
p-acetaminophenol
CC(C)=O
acetone
CC(=O)Nc1ccc(OC(C)(C)C(=O)O)cc1
2-(4-acetaminophenoxy)-2-methyl propionic acid
Rendement 60.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrea reaction scheme
  2. 2
    Autrea 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
    Autreacetone is removed under vacuum
  5. 5
    workup.DISSOLUTIONThe residue is dissolved in water (10 ml)

Mode opératoire

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-acetaminophenol in 23 g (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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05248785uspto-grants-1993_09