Réaction #2045039

ord-186d23c21cfc453899c658163c897378

Équation de réaction

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
Rendement 80.2%
O=C(O)CCCCCOc1ccc([N+](=O)[O-])cc1
6-(4-Nitrophenoxy)-hexanoic acid
Rendement 80.2%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas refluxed for 16 hours
  2. 2
    Filtrationfiltered
  3. 3
    Autredried
  4. 4
    Autrerecrystallised from a mixture of ethyl acetate:hexane (1:6)

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08409559B2uspto-grants-2013_04