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Chlorosulfonic acid → 4-Fluoro-3-iodobenzenesulfonyl chloride

HRID 2283651
ノート
印刷プレビュー

反応式

HRID 2283651 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24638Chlorosulfonic acidHCID 676731-Fluoro-2-iodobenzene

生成物 1

HCID 866823704-Fluoro-3-iodobenzenesulfonyl chloride

試薬・触媒・溶媒 1

HCID 8900Heptane溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-8047d219d85145978962a3fe58a6e321
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09145407B2

反応ノート

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