Reacción #3155

ord-2219c1d1d75847559c21756e148ff10b

Ecuación de reacción

Cl
hydrochloric acid
BrBr
bromine
[Na+].[OH-]
sodium hydroxide
CC(=O)c1ccc2c(c1)CC(C)O2
5-acetyl-2-methyl coumaran
OBr
hypobromous acid
CC1Cc2cc(C(=O)O)ccc2O1
5-carboxy-2-methylcoumaran
Rendimiento 57.4%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooling
  2. 2
    Temperaturaunder cooling on an ice bath
  3. 3
    OtroThe ice bath was removed
  4. 4
    workup.ADDITIONafter the addition
  5. 5
    workup.STIRRINGThe resultant mixture was stirred for 3.5 hours at room temperature
  6. 6
    OtroAfter the reaction
  7. 7
    Otroto precipitate a crystal
  8. 8
    FiltraciónThe crystal was recovered by filtration
  9. 9
    Lavadowashed with water
  10. 10
    OtroThe resultant crystal was dried under reduced pressure
  11. 11
    Lavadoby washing with hexane and isopropyl ether successively

Procedimiento

On an ice-common salt bath, 6.25 ml of bromine was added dropwise to a solution of 15.1 g of sodium hydroxide in 100 ml of water under stirring and cooling. To a solution of 6.50 g of 5-acetyl-2-methyl coumaran (Ml) in 100 ml of dioxane, the above mixture (i.e., hypobromous acid solution) was added dropwise at 3°-8° C. under cooling on an ice bath. The ice bath was removed after the addition. The resultant mixture was stirred for 3.5 hours at room temperature. After the reaction, the reaction mixture was poured into 500 ml of ice water, followed by addition of 30 ml of hydrochloric acid to precipitate a crystal. The crystal was recovered by filtration and washed with water. The resultant crystal was dried under reduced pressure, followed by washing with hexane and isopropyl ether successively to obtain 3.77 g of 5-carboxy-2-methylcoumaran (M2) (Yield: 57.4%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05733476uspto-grants-1998_03