Reaktion #1185895

ord-8305bf358745481cba8eb209248f7d6c

Reaktionsgleichung

COC(=O)COc1ccc([N+](=O)[O-])cc1
Methyl (4-nitrophenoxy)acetate
COC(=O)COc1ccc([N+](=O)[O-])cc1
Methyl (4-Nitro phenoxy)acetate
O=C(O)COc1ccc([N+](=O)[O-])cc1
22
Ausbeute 92.1%
O=C(O)COc1ccc([N+](=O)[O-])cc1
(4-Nitrophenoxy)acetic acid
Ausbeute 92.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationcrude 22 was filtered
  2. 2
    Sonstigedried
  3. 3
    Sonstigerecrystallised from a mixture of ethyl acetate:hexane (1:5)

Vorschrift

Methyl (4-nitrophenoxy)acetate 7 (100 g, 474 mmol) was refluxed in conc. HCl (1 L) for 8 hours. The reaction mass was cooled to room temperature and crude 22 was filtered, dried and recrystallised from a mixture of ethyl acetate:hexane (1:5) to give pure 22 (86 g, 92.1%) as a white shining powder with an m.p. between 186-188.5° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08143325B2uspto-grants-2012_03