Reacción #2045039

ord-186d23c21cfc453899c658163c897378

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas refluxed for 16 hours
  2. 2
    Filtraciónfiltered
  3. 3
    Otrodried
  4. 4
    Otrorecrystallised from a mixture of ethyl acetate:hexane (1:6)

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08409559B2uspto-grants-2013_04