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Chlorosulfonic acid → 4-Fluoro-3-iodobenzenesulfonyl chloride

HRID 2283651
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HRID 2283651 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[I:8].[Cl:9][S:10](O)(=[O:12])=[O:11]>CCCCCCC>[F:1][C:2]1[C:3]([I:8])=[CH:4][C:5]([S:10]([Cl:9])(=[O:12])=[O:11])=[CH:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 24638Chlorosulfonic acidHCID 676731-Fluoro-2-iodobenzene

생성물 1

HCID 866823704-Fluoro-3-iodobenzenesulfonyl chloride

시약·촉매·용매 1

HCID 8900Heptane용매

실험 절차

2-Fluoroiodobenzene (0.58 mL, 5.0 mmol) was added dropwise to chlorosulfonic acid (1.66 mL, 25 mmol) at 0° C. The reaction mixture was allowed to warm to ambient temperature and stirred for 2 hours. The reaction mixture was poured into ice and the mixture was extracted with dichloromethane (3×30 mL). The combined organic layer was dried over magnesium sulfate and concentrated in vacuo to obtain a crude residue. The crude residue was dissolved in heptane (100 mL) and the suspension was filtered. The filtrate was concentrated in vacuo to afford the title compound.

후처리

  1. additionThe reaction mixture was poured into ice
  2. extractionthe mixture was extracted with dichloromethane (3×30 mL)
  3. dry with materialThe combined organic layer was dried over magnesium sulfate
  4. concentrationconcentrated in vacuo
  5. customto obtain a crude residue
  6. filtrationthe suspension was filtered
  7. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-8047d219d85145978962a3fe58a6e321
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09145407B2

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