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Methanol → 4-Methanesulfonylbutan-1-ol

HRID 705339
ノート
印刷プレビュー

反応式

HRID 705339 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 230286054-Methanesulfonylbutan-1-ol収率 90%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
0 °C

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-a634bda474d04a6da0b400dae054ed08
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09173887B2

反応ノート

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