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

HRID 330410
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인쇄 미리보기

반응식

HRID 330410 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

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.

후처리

  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.

출처 및 근거

ORD 기록
ord-ff8ab009a487420ea71eb7997bbd09c4
출처 데이터셋
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04895840

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