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Chlorosulfonic acid → 4-(2-Methylpropoxy)benzene-1-sulfonyl chloride

HRID 1406552
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인쇄 미리보기

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HRID 1406552 반응식
[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[CH:2]([CH3:4])[CH3:3].[Cl:12][S:13](O)(=[O:15])=[O:14]>ClCCl>[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][C:9]([S:13]([Cl:12])(=[O:15])=[O:14])=[CH:8][CH:7]=1)[CH:2]([CH3:4])[CH3:3]
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참가 물질

4

반응물 2

HCID 24638Chlorosulfonic acid2회HCID 254373(2-Methylpropoxy)benzene

생성물 1

HCID 125711294-(2-Methylpropoxy)benzene-1-sulfonyl chloride수율 28%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-45 °C

실험 절차

To a stirring solution of isobutoxybenzene (0.60 g, 4.0 mmol) in dichloromethane (5 mL) at −45° C. was added chlorosulfonic acid (0.6 mL, 9.1 mmol) dropwise, and the reaction mixture was stirred at −45° C. for 1 h. The reaction mixture was then warmed to 0° C. and additional chlorosulfonic acid (0.6 mL, 9.1 mmol) was added dropwise. The reaction mixture was then stirred at 0° C. for 1 h and poured into ice. The aqueous layer was extracted with ethyl acetate and the organic layer was dried (Na2SO4), filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (SiO2, 5-10% ethyl acetate in hexanes) to give 4-isobutoxybenzene-1-sulfonyl chloride (0.32 g, 1.1 mmol, 28%).

후처리

  1. temperatureThe reaction mixture was then warmed to 0° C.
  2. stirringThe reaction mixture was then stirred at 0° C. for 1 h
  3. additionpoured into ice
  4. extractionThe aqueous layer was extracted with ethyl acetate
  5. dry with materialthe organic layer was dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe crude residue was purified by flash chromatography (SiO2, 5-10% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-4140584514834af1a21b7d886144ff60
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916601B2

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