Reaktion #2045039

ord-186d23c21cfc453899c658163c897378

Reaktionsgleichung

COC(=O)CCCCCOc1ccc([N+](=O)[O-])cc1
6-(4-nitrophenoxy) hexanoic acid methyl ester
COC(=O)CCCCCOc1ccc([N+](=O)[O-])cc1
6-(4-Nitro-phenoxy)-hexanoic acid methyl ester
O=C(O)CCCCCOc1ccc([N+](=O)[O-])cc1
53
Ausbeute 80.2%
O=C(O)CCCCCOc1ccc([N+](=O)[O-])cc1
6-(4-Nitrophenoxy)-hexanoic acid
Ausbeute 80.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas refluxed for 16 hours
  2. 2
    Filtrationfiltered
  3. 3
    Sonstigedried
  4. 4
    Sonstigerecrystallised from a mixture of ethyl acetate:hexane (1:6)

Vorschrift

A mixture of 6-(4-nitrophenoxy) hexanoic acid methyl ester 39 (125 g, 468.16 mmol) and concentrated HCl (1250 ml) was refluxed for 16 hours. The reaction mixture was cooled to room temperature, filtered, dried and recrystallised from a mixture of ethyl acetate:hexane (1:6) to get pure 53 (95 g, 80.2%) as a white powder. M.p: 104-107° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08409559B2uspto-grants-2013_04