Reaktion #2492376

ord-ba1644c5eeaa47b8b4db5b46c369b93e

Reaktionsgleichung

COC(=O)COc1ccc([N+](=O)[O-])cc1
methyl (4-Nitro phenoxy)acetate
COC(=O)COc1ccc([N+](=O)[O-])cc1
Methyl (4-Nitro phenoxy)acetate
O=C(O)COc1ccc([N+](=O)[O-])cc1
94
Ausbeute 92.1%
O=C(O)COc1ccc([N+](=O)[O-])cc1
(4-Nitro phenoxy)acetic acid
Ausbeute 92.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas refluxed for 8 hours
  2. 2
    FiltrationCrude 94 was filtered
  3. 3
    Sonstigedried
  4. 4
    Sonstigerecrystallized from a mixture of Ethyl acetate:Hexane (1:5)

Vorschrift

A mixture of methyl (4-Nitro phenoxy)acetate 93 (100 grams, 474 mmol) and concentrated HCl (1000 mL) was refluxed for 8 hours. The reaction mass was cooled to room temperature. Crude 94 was filtered, dried, and recrystallized from a mixture of Ethyl acetate:Hexane (1:5) to give pure 94 (86 grams, 92.1%) as a white shining powder. M.p: 186-188.5° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08802892B2uspto-grants-2014_08