Water → 5-Methanesulfonylthiophene-2-carboxylic acid

HRID 357741노트

반응식

HRID 357741 반응식
[CH3:1][S:2][C:3]1[S:7][C:6]([CH:8]=[O:9])=[CH:5][CH:4]=1.P([O-])(O)(O)=[O:11].[Na+].Cl([O-])=O.[Na+].S([O-])([O-])=O.[Na+].[Na+].[OH-:26].[Na+].[OH2:28]>C(#N)C.OO>[CH3:1][S:2]([C:3]1[S:7][C:6]([C:8]([OH:11])=[O:9])=[CH:5][CH:4]=1)(=[O:28])=[O:26]

참가 물질

9

반응물 6

HCID 962Water2회HCID 14798Sodium HydroxideHCID 24437Sodium SulfiteHCID 27369975-(Methylsulfanyl)thiophene-2-carbaldehydeHCID 23668197Sodium ChloriteHCID 23672064Monosodium phosphate

생성물 1

HCID 27404975-Methanesulfonylthiophene-2-carboxylic acid

시약·촉매·용매 2

HCID 784Hydrogen Peroxide용매HCID 6342Acetonitrile용매

실험 절차

5-Methylthio-2-thiophenecarbaldehyde (4.48 g) (synthesized in accordance with the method described in Tetrahydron, 41, 3803 (1985)) was dissolved in acetonitrile (20 ml), and sodium dihydrogen phosphate (1.2 g) in water (10 ml) and 30% aqueous hydrogen peroxide (3.5 ml) were added. Further sodium chlorite (3.85 g) in water (10 ml) was added dropwise under ice-cooling. The mixture was stirred at room temperature for 15 hours, and sodium sulfite (1 g) was added. The mixture was alkalified with 1N aqueous sodium hydroxide and extracted with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-diisopropyl ether to give 5-methanesulfonyl-2-thiphenecarboxylic acid (1.73 g) as crystals.

후처리

  1. temperaturecooling
  2. extractionextracted with diethyl ether
  3. extractionextracted with ethyl acetate
  4. dry with materialThe extract was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was recrystallized from ethyl acetate-diisopropyl ether

출처 및 근거

ORD 기록
ord-b1df5942a1d24aaea02ea1320bbdd56c
출처 데이터셋
uspto-grants-1998_11
특허 번호
US05840917

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