Реакция #3155

ord-2219c1d1d75847559c21756e148ff10b

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураcooling
  2. 2
    Температураunder cooling on an ice bath
  3. 3
    ДругоеThe 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
    ДругоеAfter the reaction
  7. 7
    Другоеto precipitate a crystal
  8. 8
    ФильтрацияThe crystal was recovered by filtration
  9. 9
    Промывкаwashed with water
  10. 10
    ДругоеThe resultant crystal was dried under reduced pressure
  11. 11
    Промывкаby washing with hexane and isopropyl ether successively

Методика

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%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05733476uspto-grants-1998_03