Реакция #684951

ord-d0dd117975bb4f1fa1b0064a511fcf44

Уравнение реакции

[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
Выход 90.1%
CCCc1ccc(CO)cc1
(4-Propylphenyl)methanol
Выход 90.1%

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe temperature of the reaction system below 20° C.
  2. 2
    workup.ADDITIONwere added
  3. 3
    Экстракцияthis mixture was extracted with ethyl acetate
  4. 4
    ПромывкаThe ethyl acetate layer was washed with saturated brine
  5. 5
    Сушкаdried over anhydrous magnesium sulfate
  6. 6
    Концентрированиеconcentrated under reduced pressure

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07897387B2uspto-grants-2011_03