Reacción #2028887

ord-9b9dc4fd40474022806e97056924a4ff

Ecuación de reacción

Cl
hydrochloric acid
CCOC=O
Ethyl formate
CC(=O)c1ccc(Cl)cc1
4′-chloroacetophenone
C[O-].[Na+]
Sodium methoxide
O=CCC(=O)c1ccc(Cl)cc1
yellow oil
Rendimiento 100.2%
O=CCC(=O)c1ccc(Cl)cc1
3-[4-(chloro)phenyl]-propane-1,3-dione
Rendimiento 100.2%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe phases were separated
  2. 2
    Lavadothe ethereal solution washed with brine
  3. 3
    Secadodried over magnesium sulfate
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated in vacuo

Procedimiento

Ethyl formate (8.15 g, 0.11 mol) and 4′-chloroacetophenone (15.4 g, 0.1 mol) were stirred in ether (150 mL) at room temperature. Sodium methoxide (25%) (23.77 g, 0.11 mol) was added dropwise. The mixture was stirred at room temperature for 16 hours and was then treated with 150 mL of 1N hydrochloric acid. The phases were separated and the ethereal solution washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo to afford 18.3 g of a yellow oil. The resulting crude mixture was used directly in the next step without purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE044048E1uspto-grants-2013_03