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Ozone → HCID 10846567、化合物

HRID 264389
ノート
印刷プレビュー

反応式

HRID 264389 の反応式
[O:1]=[O+][O-].[CH2:4]([CH:8]1[C:16]([CH3:18])([CH3:17])[C:15]2[C:10](=[CH:11][C:12]([F:19])=[CH:13][CH:14]=2)[C:9]1=[O:20])[CH:5]=CC>ClCCl.CO>[O:1]=[CH:5][CH2:4][CH:8]1[C:16]([CH3:18])([CH3:17])[C:15]2[C:10](=[CH:11][C:12]([F:19])=[CH:13][CH:14]=2)[C:9]1=[O:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 24823Ozone2 回HCID 54557992HCID 54557992、化合物

生成物 1

HCID 10846567HCID 10846567、化合物収率 95%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 6344Dichloromethane溶媒

実験手順

An ozone stream (1.5 g ozone/hour) was conducted for 30 minutes while stirring through a solution, cooled to -70°, of 3.38 g of (RS)-2-(2-buten-1-yl)-6-fluoro-3,3-dimethyl-1-indanone in 75 ml of anhydrous dichloromethane and 15 ml of anhydrous methanol. Subsequently, the mixture was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 1.6 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 40 ml of dichoromethane and, after the addition of 5 ml of water and 5 ml of trifluoroacetic acid, stirred at room temperature for 2 hours. The mixture was subsequently poured into 90 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. 3.04 g (95%) of (RS)-2-(2-oxoethyl)-6-fluoro-3,3-dimethyl-1-indanone were obtained as a light yellow oil.

後処理

  1. customSubsequently, the mixture was flushed with oxygen for 5 minutes and with argon for 10 minutes
  2. additionAfter the addition of 1.6 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 40 ml of dichoromethane
  6. additionafter the addition of 5 ml of water and 5 ml of trifluoroacetic acid
  7. stirringstirred at room temperature for 2 hours
  8. additionThe mixture was subsequently poured into 90 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

出典と根拠

ORDレコード
ord-30037145d23a4ecf84aa3396ee0eb38d
出典データセット
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05646173

反応ノート

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