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Chlorosulfonic acid → 4-Bromo-2,5-di(propan-2-yl)benzene-1-sulfonyl chloride

HRID 1973537
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인쇄 미리보기

반응식

HRID 1973537 반응식
[Br:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[CH:5]=[CH:4][C:3]=1[CH:11]([CH3:13])[CH3:12].[Cl:14][S:15](O)(=[O:17])=[O:16]>C(Cl)(Cl)(Cl)Cl>[Br:1][C:2]1[C:3]([CH:11]([CH3:13])[CH3:12])=[CH:4][C:5]([S:15]([Cl:14])(=[O:17])=[O:16])=[C:6]([CH:8]([CH3:9])[CH3:10])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24638Chlorosulfonic acidHCID 119589802-Bromo-1,4-bis(propan-2-yl)benzene

생성물 1

HCID 214920504-Bromo-2,5-di(propan-2-yl)benzene-1-sulfonyl chloride

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

To a one-liter flask containing 80 parts of 2-bromo-1,4-diisopropylbenzene in 320 parts of carbon tetrachloride, there is added over 15 min. 154 parts of chlorosulfonic acid. After stirring thirty min. longer, the reaction mixture is poured onto 1000 parts of ice. The organic layer is separated and washed with 200 parts of water and then dried over magnesium sulfate. Removal of the solvent under reduced pressure gives 105 parts of 4-bromo-2,5-diisopropylbenzenesulfonyl chloride which can be recrystallized from n-hexane, m.p. 80°-83°.

후처리

  1. additionis added over 15 min
  2. additionthe reaction mixture is poured onto 1000 parts of ice
  3. customThe organic layer is separated
  4. washwashed with 200 parts of water
  5. dry with materialdried over magnesium sulfate
  6. customRemoval of the solvent under reduced pressure

출처 및 근거

ORD 기록
ord-7e974b47a08b4f6fb4a97fdc00de500d
출처 데이터셋
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03997603

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