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Chlorosulfonic acid → 2-Fluoro-3-methyl-5-nitrobenzene-1-sulfonyl chloride

HRID 1770817
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인쇄 미리보기

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HRID 1770817 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[CH3:11].[Cl:12][S:13](O)(=[O:15])=[O:14]>>[Cl:12][S:13]([C:7]1[CH:6]=[C:5]([N+:8]([O-:10])=[O:9])[CH:4]=[C:3]([CH3:11])[C:2]=1[F:1])(=[O:15])=[O:14]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24638Chlorosulfonic acidHCID 68001Benzene, 1-fluoro-2-methyl-4-nitro-

생성물 1

HCID 575628802-Fluoro-3-methyl-5-nitrobenzene-1-sulfonyl chloride

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온도
110 °C

실험 절차

A dry reaction flask equipped with a stirring bar, a reflux condenser and nitrogen inlet was charged with 4-fluoro-3-methylnitrobenzene (25) (3.10 g, 20 mmol). To this at 0° C., was added dropwise chlorosulfonic acid (5.29 mL, 80 mmol) over a period of 15 minutes. After bringing the homogeneous solution to room temperature, it was stirred at 110° C. for 24 hours. The resulting slurry was then poured over ice water (100 gm), extracted with diethyl ether (3×75 mL), and the organic phase washed with water (75 mL), then dried over anhydrous sodium sulfate. The solvent was then removed under reduced pressure to afford the corresponding sulfonyl chloride derivative (26), which was used further without purification.

후처리

  1. customA dry reaction flask
  2. customequipped with a stirring bar, a reflux condenser and nitrogen inlet
  3. customto room temperature
  4. extractionextracted with diethyl ether (3×75 mL)
  5. washthe organic phase washed with water (75 mL)
  6. dry with materialdried over anhydrous sodium sulfate
  7. customThe solvent was then removed under reduced pressure

출처 및 근거

ORD 기록
ord-156d13b598d0456fa7e5ad6941e87e52
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09248190B2

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