Reacción #725910

ord-6c566cbc9ab746a8a9126547a6df3a8e

Ecuación de reacción

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
39
Rendimiento 65.2%
COC(=O)CCCCCOc1ccc([N+](=O)[O-])cc1
6-(4-Nitro-phenoxy)-hexanoic acid methyl ester
Rendimiento 65.2%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaheated
  2. 2
    Temperaturato reflux for 48 hours
  3. 3
    workup.DISTILLATIONAcetone was distilled off
  4. 4
    workup.ADDITIONwater (2 L) was added
  5. 5
    FiltraciónCrude 39 was filtered
  6. 6
    Otrodried
  7. 7
    Otrorecrystallised from a mixture of ethyl acetate:hexane (1:6)

Procedimiento

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) and heated to reflux for 48 hours. Acetone was distilled off and water (2 L) was added. Crude 39 was filtered, dried and recrystallised from a mixture of ethyl acetate:hexane (1:6) to get pure 39 (130 g, 45.1%) as a white powder. M.p: 84.5.5-86.6° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07691364B2uspto-grants-2010_04