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Hydrogen Peroxide → 2-Sec-butylsulfinyl-4-methylsulfonyloxy-1,3-thiazole

HRID 414255
ノート
印刷プレビュー

反応式

HRID 414255 の反応式
[CH:1]([S:5][C:6]1[S:7][CH:8]=[C:9]([O:11][S:12]([CH3:15])(=[O:14])=[O:13])[N:10]=1)([CH2:3][CH3:4])[CH3:2].[OH:16]O.O.[OH-].[Na+]>C(O)(=O)C>[CH:1]([S:5]([C:6]1[S:7][CH:8]=[C:9]([O:11][S:12]([CH3:15])(=[O:13])=[O:14])[N:10]=1)=[O:16])([CH2:3][CH3:4])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 784Hydrogen PeroxideHCID 962WaterHCID 14798Sodium HydroxideHCID 13914052HCID 13914052、化合物

生成物 1

HCID 139140652-Sec-butylsulfinyl-4-methylsulfonyloxy-1,3-thiazole収率 49.7%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

4.0 g of 2-sec-butylthio-4-methylsulfonyloxy-1,3-thiazole was dissolved in 15 ml of acetic acid, and 2.2 ml of 35% aqueous hydrogen peroxide was added to the solution at room temperature, followed by reaction at 30° to 40° C. for 4 hours. The reaction mixture was poured into chilled water, neutralized by 5% aqueous solution of sodium hydroxide, and extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of common salt, dried over anhydrous sodium sulfate and concentrated to obtain an oil, which was purified by silica-gel column chromatography to 2.1 g of the objective compound as a pale yellow oil (yield: 49.7%).

後処理

  1. customfollowed by reaction at 30° to 40° C. for 4 hours
  2. additionThe reaction mixture was poured
  3. extractionextracted with ethyl acetate
  4. washThe extract was washed with a saturated aqueous solution of common salt
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated
  7. customto obtain an oil, which

出典と根拠

ORDレコード
ord-dc4efc705ded4ed89938438e52e9c97d
出典データセット
uspto-grants-1988_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04791127

反応ノート

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