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Dichloromethane → 5-tert-Butyl-2-methylbenzene-1-sulfonyl chloride

HRID 543371
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인쇄 미리보기

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HRID 543371 반응식
[CH3:1][C:2]([C:5]1[CH:10]=[CH:9][C:8](O)=[CH:7][CH:6]=1)([CH3:4])[CH3:3].[Cl:12][S:13]([OH:16])(=O)=[O:14].[CH2:17](Cl)Cl>>[CH3:1][C:2]([C:5]1[CH:10]=[C:9]([S:13]([Cl:12])(=[O:16])=[O:14])[C:8]([CH3:17])=[CH:7][CH:6]=1)([CH3:4])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6344Dichloromethane2회HCID 73934-tert-ButylphenolHCID 24638Chlorosulfonic acid

생성물 1

HCID 51688795-tert-Butyl-2-methylbenzene-1-sulfonyl chloride

실험 절차

12.3 g (0.075 mol) of 4-(1,1-dimethylethyl)phenol in 30 ml of methylene chloride are added dropwise, cooling in ice, to 16.5 ml of chlorosulfonic acid dissolved in 20 ml of methylene chloride. The mixture is stirred for 40 minutes and then poured onto ice-water. The organic phase is separated off, washed with water, dried with MgSO4 and evaporated. The product is recrystallized from toluene petroleum ether.

후처리

  1. additionpoured onto ice-water
  2. customThe organic phase is separated off
  3. washwashed with water
  4. dry with materialdried with MgSO4
  5. customevaporated
  6. customThe product is recrystallized from toluene petroleum ether

출처 및 근거

ORD 기록
ord-c4399c49ebf2467a9128d8151eef1df5
출처 데이터셋
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04661636

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