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Methanol → 4-Methanesulfonylbutan-1-ol

HRID 705339
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인쇄 미리보기

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HRID 705339 반응식
CS[CH2:3][CH2:4][CH2:5][CH2:6][OH:7].[OH:8][S:9]([O-:12])(=O)=O.[K+].[CH3:14]O>O>[CH3:14][S:9]([CH2:3][CH2:4][CH2:5][CH2:6][OH:7])(=[O:12])=[O:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 516920Potassium bisulfateHCID 5197934-(Methylthio)butanol

생성물 1

HCID 230286054-Methanesulfonylbutan-1-ol수율 90%

시약·촉매·용매 1

HCID 962Water용매

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온도
0 °C

실험 절차

4-(Methylthio)butan-1-ol (721 mg, 6.0 mmol) was dissolved in methanol (15 mL) and cooled to 0° C. in an ice bath. 2KHSO5.KHSO4.K2SO4 (4057 mg, 6.60 mmol), dissolved in water (15 mL), was added dropwise over a 10 minute period. Upon completion of addition, the reaction mixture was removed from the ice bath and warmed to room temperature and stirred for one hour. The reaction mixture was diluted with water (15 mL) and extracted with ethyl acetate (50 mL). The aqueous layer was concentrated to dryness, and the residue was diluted with dichloromethane, stirred 30 minutes and filtered. The filtrate was concentrated to give the title compound as a clear oil (825 mg, 90%).

후처리

  1. additionwas added dropwise over a 10 minute period
  2. additionUpon completion of addition
  3. customthe reaction mixture was removed from the ice bath
  4. temperaturewarmed to room temperature
  5. additionThe reaction mixture was diluted with water (15 mL)
  6. extractionextracted with ethyl acetate (50 mL)
  7. concentrationThe aqueous layer was concentrated to dryness
  8. additionthe residue was diluted with dichloromethane
  9. stirringstirred 30 minutes
  10. filtrationfiltered
  11. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-a634bda474d04a6da0b400dae054ed08
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09173887B2

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