Reacción #41956

ord-50fe9b92db544c87abd868a71e54946d

Ecuación de reacción

CCOC(CCl)OCC
Chloroacetaldehyde diethyl acetal
O=C([O-])c1ccccc1.[K+]
potassium benzoate
[Br-].[K+]
potassium bromide
CN(C)C=O
DMF
CCOC(COC(=O)c1ccccc1)OCC
compound
Rendimiento 34.1%
CCOC(COC(=O)c1ccccc1)OCC
2-benzoyloxyacetaldehyde Diethyl Acetal
Rendimiento 34.1%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaby refluxing
  2. 2
    FiltraciónAfter filtration
  3. 3
    Lavadothe organic layer was washed with water (30 mL)
  4. 4
    Secadowas dried over anhydrous sodium sulfate
  5. 5
    FiltraciónSubsequent filtration and vacuum concentration

Procedimiento

Chloroacetaldehyde diethyl acetal (2.00 g), potassium benzoate (1.91 g), potassium bromide (0.30 g) and DMF (20 mL) were placed in a three-neck flask, followed by refluxing. Twenty hours later, the reaction mixture was cooled to room temperature, and water (30 mL) and ethyl acetate (80 mL) were added thereto, followed by stirring. After filtration, the organic layer was washed with water (30 mL) and was dried over anhydrous sodium sulfate. Subsequent filtration and vacuum concentration yielded the target compound (0.97 g) in a yield of 31%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07728152B2uspto-grants-2010_06