Reaktion #589024

ord-870c51f8df9d4d22876604cf77809c32

Reaktionsgleichung

COC(=O)CCCCCBr
methyl 6-bromohexanoate
O=[N+]([O-])c1ccc(O)cc1
4-nitrophenol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
[I-].[Na+]
sodium iodide
COC(=O)CCCCCOc1ccc([N+](=O)[O-])cc1
21
Ausbeute 65.2%
COC(=O)CCCCCOc1ccc([N+](=O)[O-])cc1
6-(4-Nitrophenoxy)-hexanoic acid methyl ester
Ausbeute 65.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturheating
  2. 2
    Temperaturto reflux for 48 hours
  3. 3
    workup.DISTILLATIONAcetone was distilled off
  4. 4
    workup.ADDITIONwater (2 L) was added
  5. 5
    FiltrationCrude 21 was filtered
  6. 6
    Sonstigedried
  7. 7
    Sonstigerecrystallised from a mixture of ethyl acetate:hexane (1:6)

Vorschrift

To a mixture of 4-nitrophenol (150 g, 1.079 moles), potassium carbonate (600 g, 4.341 moles) and sodium iodide (10 g, 66.7 mmol) in anhydrous acetone (2.1 L) was added methyl 6-bromohexanoate (156 g, 746.41 mmol) with and heating to reflux for 48 hours. Acetone was distilled off and water (2 L) was added. Crude 21 was filtered, dried and recrystallised from a mixture of ethyl acetate:hexane (1:6) to get pure 21 (130 g, 45.1%) as a white powder with an m.p. between 84.5.5-86.6° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07772352B2uspto-grants-2010_08