反応 #3155

ord-2219c1d1d75847559c21756e148ff10b

反応方程式

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
収率 57.4%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooling
  2. 2
    温度under cooling on an ice bath
  3. 3
    その他The 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
    その他After the reaction
  7. 7
    その他to precipitate a crystal
  8. 8
    ろ過The crystal was recovered by filtration
  9. 9
    洗浄washed with water
  10. 10
    その他The resultant crystal was dried under reduced pressure
  11. 11
    洗浄by washing with hexane and isopropyl ether successively

実験手順

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%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05733476uspto-grants-1998_03