Reaktion #158529

ord-3c5b8c562bf8420d839ba18c1bd1c9f2

Reaktionsgleichung

O=[N+]([O-])c1cccc(O)c1
3-Nitrophenol
COC(=O)c1ccc(CCl)o1
methyl 5-(chloromethyl)-2-furoate
O=C([O-])[O-].[K+].[K+]
K2CO3
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
desired product
Ausbeute 90.8%
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
4-(4-nitrophenoxymethyl)-2-methoxycarbonyl-furan
Ausbeute 90.8%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was cooled
  2. 2
    FiltrationThe resultant white solid was filtered
  3. 3
    Waschenwashed with water and air
  4. 4
    Sonstigedried overnight

Vorschrift

3-Nitrophenol (1.0 g, 7.19 mmole), methyl 5-(chloromethyl)-2-furoate (1.38 g, 7.90 mmole) and anhydrous K2CO3 (1.19 g, 8.60 mmole) in acetone (30 mL) were refluxed for 8 h. The reaction mixture was cooled and diluted with water. The resultant white solid was filtered, washed with water and air dried overnight to give 1.81 g (90%) of the desired product. 1H NMR (CDCl3): δ 7.86 (dd, 1H, J=2.3 and 8.2 Hz), 7.80 (t, 1H, J=2.3 Hz), 7.45 (t, 1H, J=8.2 Hz), 7.27 (dd, 1H, J=2.3 and 8.2 Hz), 7.17 (d, 1H, J=3.5 Hz), 6.58 (d, 1H, J=3.5 Hz), 5.13 (s, 2H), 3.90 (s, 3H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08822685B2uspto-grants-2014_09