Chlorosulfonic acid → 1261827-78-4
Reaction equation
[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]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
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.
Workup
- additionThe reaction mixture was poured into ice
- extractionthe mixture was extracted with dichloromethane (3×30 mL)
- dry with materialThe combined organic layer was dried over magnesium sulfate
- concentrationconcentrated in vacuo
- customto obtain a crude residue
- filtrationthe suspension was filtered
- concentrationThe filtrate was concentrated in vacuo
Sources & evidence
- ORD record
- ord-8047d219d85145978962a3fe58a6e321
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09145407B2
Reaction notes
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