Reacción #2069944

ord-4ac04bc31f104175a45a5a3b8cd546f2

Ecuación de reacción

[Na+].[OH-]
sodium hydroxide
[BH4-].[Na+]
sodium borohydride
O=S(=O)(O)O
sulfuric acid
CCCc1ccc(C(=O)O)cc1
p-n-propylbenzoic acid
CCCc1ccc(CO)cc1
title compound
Rendimiento 90.1%
CCCc1ccc(CO)cc1
(4-Propylphenyl)methanol
Rendimiento 90.1%

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe temperature of the reaction system below 20° C.
  2. 2
    workup.ADDITIONwere added
  3. 3
    Extracciónthis mixture was extracted with ethyl acetate
  4. 4
    LavadoThe ethyl acetate layer was washed with saturated brine
  5. 5
    Secadodried over anhydrous magnesium sulfate
  6. 6
    Concentraciónconcentrated under reduced pressure

Procedimiento

A solution of sodium borohydride (2.9 g, 76 mmol) and concentrated sulfuric acid in ether (prepared by adding 2.0 ml of concentrated sulfuric acid to 4.0 ml of ether) was added dropwise to a solution of p-n-propylbenzoic acid (5.0 g, 32 mmol) in tetrahydrofuran (20 ml) cooled to 0° C. keeping the temperature of the reaction system below 20° C., and then this mixture was stirred at room temperature for 3 hours. After the mixture was cooled on ice, methanol and 1 N sodium hydroxide were added, and this mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure to give the title compound (4.33 g). This compound was used in the following reaction without purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07541332B2uspto-grants-2009_06