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Ozone → (RS)-2-(2-oxoethyl)-6-tert-butyl-1-indanone

HRID 264488
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HRID 264488 반응식
[O:1]=[O+][O-].[CH2:4]([CH:8]1[CH2:16][C:15]2[C:10](=[CH:11][C:12]([C:17]([CH3:20])([CH3:19])[CH3:18])=[CH:13][CH:14]=2)[C:9]1=[O:21])[CH:5]=CC>ClCCl.CO>[O:1]=[CH:5][CH2:4][CH:8]1[CH2:16][C:15]2[C:10](=[CH:11][C:12]([C:17]([CH3:20])([CH3:19])[CH3:18])=[CH:13][CH:14]=2)[C:9]1=[O:21]
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참가 물질

5

반응물 2

HCID 24823Ozone2회HCID 53952129(RS)-2-(2-buten-1-yl)-6-tert-butyl-1-indanone

생성물 1

HCID 19036442(RS)-2-(2-oxoethyl)-6-tert-butyl-1-indanone수율 92%

시약·촉매·용매 2

HCID 887Methanol용매HCID 6344Dichloromethane용매

실험 절차

An ozone stream (3 g ozone/hour) was conducted for 35 minutes while stirring through a solution, cooled to -70°, of 7.35 g of (RS)-2-(2-buten-1-yl)-6-tert-butyl-1-indanone in 150 ml of anhydrous dichloromethane and 30 ml of anhydrous methanol. Subsequently, the solution was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 3.36 ml of dimethyl sulfide, the mixture was stirred at room temperature for 17 hours. The reaction mixture was evaporated in a vacuum. The residue was treated with 100 ml of dichoromethane and, after the addition of 15 ml of water and 15 ml of trifluoroacetic acid, stirred at room temperature for 3 hours. The mixture was subsequently poured into 100 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 150 ml of dichloromethane each time. The combined organic phases were dried over magnesium sulfate and concentrated in a vacuum. 6.44 g (92%) of (RS)-2-(2-oxoethyl)-6-tert-butyl-1-indanone were obtained as a yellow oil.

후처리

  1. customSubsequently, the solution was flushed with oxygen for 5 minutes and with argon for 10 minutes
  2. additionAfter the addition of 3.36 ml of dimethyl sulfide
  3. stirringthe mixture was stirred at room temperature for 17 hours
  4. customThe reaction mixture was evaporated in a vacuum
  5. additionThe residue was treated with 100 ml of dichoromethane
  6. additionafter the addition of 15 ml of water and 15 ml of trifluoroacetic acid
  7. stirringstirred at room temperature for 3 hours
  8. additionThe mixture was subsequently poured into 100 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 150 ml of dichloromethane each time
  14. dry with materialThe combined organic phases were dried over magnesium sulfate
  15. concentrationconcentrated in a vacuum

출처 및 근거

ORD 기록
ord-e128150ecf21427191a4bff074780c4c
출처 데이터셋
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05646173

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