Реакция #2028884

ord-86e9ef1581f54ccbaf93858808191b56

Уравнение реакции

Cl
HCl
C[O-].[Na+]
sodium methoxide
CCOC(=O)C(F)(F)F
Ethyl trifluoroacetate
Cc1ccc2c(c1)CCCC2=O
6-methyltetralone
Cc1ccc2c(c1)CCC(C(=O)C(F)(F)F)C2=O
oil
Выход 85.1%
Cc1ccc2c(c1)CCC(C(=O)C(F)(F)F)C2=O
6-methyl-2-(trifluoroacetyl)tetralone
Выход 85.1%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe organic layer was collected
  2. 2
    Промывкаwashed with brine
  3. 3
    Сушкаdried over MgSO4
  4. 4
    Концентрированиеconcentrated in vacuo

Методика

Ethyl trifluoroacetate (5.33 g, 37.5 mmol) was dissolved in ether (50 mL) and treated with a sodium methoxide solution (25% in methanol, 9.92 g, 45.9 mmol) followed by 6-methyltetralone (5.94 g, 37.1 mmol). The reaction was stirred at room temperature for 6.1 hours then treated with 1N HCl (20 mL). The organic layer was collected, washed with brine, dried over MgSO4, and concentrated in vacuo to give a brown oil (8.09 g) that was used in the next step without further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE044048E1uspto-grants-2013_03