HRID264417

反应详情

EQUATION

反应方程式

HRID 264417 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

An ozone stream (2 g ozone/hour) was conducted for 90 minutes while stirring through a solution, cooled to -70°, of 5.1 g of (RS)-2-(2-buten-1-yl)-6-isobutoxy-1-indanone in 150 ml of anhydrous dichloromethane and 30 ml of anhydrous methanol. Subsequently, the mixture was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 2.16 ml of dimethyl sulfide, the mixture was stirred at room temperature for 15 hours. The reaction mixture was evaporated in a vacuum, the residue was treated with 170 ml of dichoromethane and, after the addition of 25 ml of water and 25 ml of trifluoroacetic acid, stirred at room temperature for 3 hours. The mixture was subsequently poured into 150 ml of water and neutralized by the spatula-wise addition of sodium hydrogen carbonate while stirring. An additional 50 ml of water were added. The phases were separated and the aqueous phase was extracted twice with 100 ml of dichloromethane each time. The combined organic phases were dried over magnesium sulfate and concentrated in a vacuum. 2.3 g (48%) of (RS)-2-(2-oxoethyl)-6-isobutoxy-1-indanone were obtained as a red-brown oil.

WORKUP

后处理

  1. customSubsequently, the mixture was flushed with oxygen for 5 minutes and with argon for 10 minutes
  2. additionAfter the addition of 2.16 ml of dimethyl sulfide
  3. stirringthe mixture was stirred at room temperature for 15 hours
  4. customThe reaction mixture was evaporated in a vacuum
  5. additionthe residue was treated with 170 ml of dichoromethane
  6. additionafter the addition of 25 ml of water and 25 ml of trifluoroacetic acid
  7. stirringstirred at room temperature for 3 hours
  8. additionThe mixture was subsequently poured into 150 ml of water
  9. additionneutralized by the spatula-wise addition of sodium hydrogen carbonate
  10. stirringwhile stirring
  11. additionAn additional 50 ml of water were added
  12. customThe phases were separated
  13. extractionthe aqueous phase was extracted twice with 100 ml of dichloromethane each time
  14. dry with materialThe combined organic phases were dried over magnesium sulfate
  15. concentrationconcentrated in a vacuum