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2-[4-(Methylthio)phenoxy]ethanol → Ethanol, 2-[4-(methylsulfonyl)phenoxy]-

HRID 330410
ノート
印刷プレビュー

反応式

HRID 330410 の反応式
CS[C:3]1[CH:12]=[CH:11][C:6]([O:7][CH2:8][CH2:9][OH:10])=[CH:5][CH:4]=1.Cl[C:14]1C(C2C=CC=CC=2)=C(C=CC=1)C(O)=O.[S:29](=[O:32])(O)[O-:30].[Na+]>C(Cl)Cl>[CH3:14][S:29]([C:3]1[CH:12]=[CH:11][C:6]([O:7][CH2:8][CH2:9][OH:10])=[CH:5][CH:4]=1)(=[O:32])=[O:30]
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 3

HCID 148552542-[4-(Methylthio)phenoxy]ethanolHCID 23665763Sodium BisulfiteHCID 46314701m-Chlorophenylbenzoic acid

生成物 1

HCID 14855255Ethanol, 2-[4-(methylsulfonyl)phenoxy]-

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A solution of 14.1 g (0.77 mole) of 2-[4-(methylthio)phenoxy]ethanol (from Preparation 35) and 31.2 g (0.18 mole) of m-chlorophenylbenzoic acid in 800 ml of methylene chloride was stirred at room temperature overnight. A saturated, aqueous solution (300 ml) of sodium bisulfite was added, and the mixture was stirred at room temperature for 0.5 hr. The phases were separated, the mthylene chloride solution was dried over magnesium sulfate, and the volume reduced to approximately 100 ml in vacuo. n-Hexane was added until the solution became cloudy, and 9.40 g (56.8%) of the product precipitated as a white, crystalline solid, m.p. 96°-98° C.

後処理

  1. customThe phases were separated
  2. dry with materialthe mthylene chloride solution was dried over magnesium sulfate
  3. additionn-Hexane was added until the solution
  4. customprecipitated as a white, crystalline solid, m.p. 96°-98° C.

出典と根拠

ORDレコード
ord-ff8ab009a487420ea71eb7997bbd09c4
出典データセット
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04895840

反応ノート

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