Iodine → 6,7-Dichloro-4-formylquinoline

HRID 599357

Reaktionsgleichung

Reaktionsgleichung von HRID 599357
F[C:2](F)(F)[C:3]([OH:5])=O.C(I)(C)(C)C.II.[Cl:15][C:16]1[CH:17]=[C:18]2[C:23](=[CH:24][C:25]=1[Cl:26])[N:22]=[CH:21][CH:20]=C2C.S([O-])([O-])(=O)=S.[Na+].[Na+].C(=O)([O-])O.[Na+]>CS(C)=O.O.O.O.O.[Fe](Cl)Cl.C(OCC)(=O)C>[Cl:15][C:16]1[CH:17]=[C:18]2[C:23](=[CH:24][C:25]=1[Cl:26])[N:22]=[CH:21][CH:20]=[C:2]2[CH:3]=[O:5]

Komponenten

10

Versuchsvorschrift

Trifluoroacetic acid (360 μL, 4.7 mmol), tert-butyl iodide (450 μL, 3.8 mmol), iodine (990 mg, 3.9 mmol) and iron(II) chloride tetrahydrate (170 mg, 0.85 mmol) were added sequentially to a solution of 6,7-dichloro-4-methylquinoline (Reference compound No. 1-2, 790 mg, 3.7 mmol) in dimethylsulfoxide (18 mL) at room temperature, and the mixture was stirred at 80° C. for 7 hours. Then saturated sodium thiosulfate aqueous solution (100 mL) was added, and then ethyl acetate (300 mL) and saturated aqueous sodium hydrogencarbonate solution (200 mL) were added thereto. The mixture was separated into the organic layer and the aqueous layer, and the organic layer was washed with saturated brine (100 mL), dried over anhydrous magnesium sulfate, The solvent was evaporated under reduced pressure to give 840 mg of the title reference compound as a brown solid (Yield: 99%).

Aufarbeitung

  1. customThe mixture was separated into the organic layer
  2. washthe aqueous layer, and the organic layer was washed with saturated brine (100 mL)
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe solvent was evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-ef43c900f8c9448a885bb5d4533180fa
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07897774B2

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