Reaktion #574069

ord-b322282564e2445ca2b0a3b949d6007f

Reaktionsgleichung

Cl
HCl
O
water
CC(C)(Oc1ccc(N)cc1)C(=O)O
2-(4-aminophenoxy)-2-methylpropionic acid
O=C=Nc1cc(Cl)cc(Cl)c1
3,5-dichlorophenyl isocyanate
CC(C)(Oc1ccc(NC(=O)Nc2cc(Cl)cc(Cl)c2)cc1)C(=O)O
2-(4-(3,5-Dichlorophenylureido)phenoxy)-2-methylpropionic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe precipitate was filtered
  2. 2
    Waschenwashed several times with cold water
  3. 3
    Sonstigedried
  4. 4
    SonstigeRecrystallization from aqueous acetone
  5. 5
    Sonstigegave small plates 1.81 g (94%) MP 182°-184°

Vorschrift

To a stirring solution of 4.95 g (0.025 mole) of 2-(4-aminophenoxy)-2-methylpropionic acid in 50 ml dry pyridine, 4.95 g (0.025 mole) of 3,5-dichlorophenyl isocyanate were added. After 1 hour stirring at room temperature, 150 ml water was added and the mixture was acidified with concentrated HCl. The precipitate was filtered, washed several times with cold water and dried. Recrystallization from aqueous acetone gave small plates 1.81 g (94%) MP 182°-184°.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05292935uspto-grants-1994_03