Reacción #1375813

ord-871560983abd480daa5fe2479ef7f7f5

Ecuación de reacción

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccc(C(=O)OC)cc1
methyl 4-tri-n-butylstannylbenzoate
[K+].[OH-]
KOH
CC(=O)O
acetic acid
O
water
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccc(C(=O)O)cc1
title compound
Rendimiento 90.3%
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccc(C(=O)O)cc1
4-Tri-n-butylstannylbenzoic acid
Rendimiento 90.3%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe resulting solution was refluxed for 2 hours
  2. 2
    TemperaturaThe solution was cooled
  3. 3
    ExtracciónThe solution was then extracted with diethyl ether (80 ml)
  4. 4
    LavadoThe ether phase was washed with water (30 ml)
  5. 5
    Secadodried over MgSO4 (5 g)
  6. 6
    Filtraciónfiltered
  7. 7
    Otroevaporated under reduced pressure

Procedimiento

To a solution of methyl 4-tri-n-butylstannylbenzoate (3.0 g, 7 mmol) in absolute ethanol (60 ml) was added 0.25 g KOH (9 mmol). The resulting solution was refluxed for 2 hours. The solution was cooled and poured into an ice-cold solution of acetic acid (0.64 g, 10.6 mmol) and water (100 ml). The solution was then extracted with diethyl ether (80 ml). The ether phase was washed with water (30 ml), dried over MgSO4 (5 g), filtered and evaporated under reduced pressure to afford 2.6 g (88%) of the title compound. This material was used without further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05746997uspto-grants-1998_05