Реакция #417932

ord-65cf5a608b55415d88d1bb6eb4d45d64

Уравнение реакции

Cl
HCl
CC(CC(=O)Cl)c1ccccc1
3-phenylbutanoyl chloride
Oc1ccccc1
phenol
c1ccncc1
pyridine
CC(CC(=O)Oc1ccccc1)c1ccccc1
colourless oil
Выход 83.8%
CC(CC(=O)Oc1ccccc1)c1ccccc1
Phenyl 3-phenylbutanoate
Выход 83.8%

Растворители

Условия реакции

Температура
10°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGThe mixture was stirred intensely for 15 min
  2. 2
    Другоеtransferred into a separatory funnel
  3. 3
    ДругоеThe aqueous layer was separated
  4. 4
    Промывкаthe organic layer washed 4 times with water
  5. 5
    Сушкаbrine and dried over MgSO4
  6. 6
    ДругоеThe solvent was removed in a rotary evaporator
  7. 7
    workup.DISTILLATIONthe residue short-path distilled at 125-128° C./0.07 mbar

Методика

To the solution of phenol (8.62 g, 92 mmol) and 4-dimethylaminopyridine (400 mg) in toluene (110 ml) was added pyridine (18.1 g, 229 mmol) and the resulting solution was cooled to 10° C. Then a solution of 3-phenylbutanoyl chloride (20.1 g, 110 mmol) was added dropwise. The resulting mixture was stirred at room temperature for 24 h, and then cooled to 5° C. before the careful addition of 2N aq. HCl-solution (225 ml). The mixture was stirred intensely for 15 min, then diluted with toluene and transferred into a separatory funnel. The aqueous layer was separated and the organic layer washed 4 times with water, then brine and dried over MgSO4. The solvent was removed in a rotary evaporator and the residue short-path distilled at 125-128° C./0.07 mbar to yield 18.52 g (70%) of colourless oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08877704B2uspto-grants-2014_11