Reaktion #74677
ord-43cb9afef6fd4e369f6691015b6df7f0
Reaktionsgleichung
Reaktionsbedingungen
Aufarbeitung
- 1workup.ADDITIONAfter addition
- 2FiltrationThe reaction mixture was filtered through diatomaceous earth
- 3Waschenthe filtrate was washed successively with 10% aqueous sodium thiosulfate (w/v), half-saturated aqueous sodium bicarbonate, water and brine
- 4TrocknenThe organic phase was dried over sodium sulfate
- 5Filtrationfiltered
- 6Einengenconcentrated onto diatomaceous earth
- 7SonstigeThe residue was purified by automated flash chromatography (24 g SiO2, hexanes to 1:1 methylene chloride-hexanes gradient elution)
- 8workup.ADDITIONThe initial product-containing fraction
- 9EinengenThe remaining fractions were concentrated in vacuo
Vorschrift
A solution of iodine (0.874 g, 3.44 mmol) in chloroform (17.1 mL, 214 mmol) was added over a period of 1.5 hours dropwise via addition funnel to a mixture of 3-fluoro-4-(trifluoromethyl)phenol (Preparation 886, 620 mg, 3.4 mmol) and silver trifluoroacetate (0.760 g, 3.44 mmol) in chloroform (3.4 mL, 43 mmol). After addition was complete, the reaction mixture was stirred an additional 1 hour. The reaction mixture was filtered through diatomaceous earth, and the filtrate was washed successively with 10% aqueous sodium thiosulfate (w/v), half-saturated aqueous sodium bicarbonate, water and brine. The organic phase was dried over sodium sulfate, filtered, and concentrated onto diatomaceous earth. The residue was purified by automated flash chromatography (24 g SiO2, hexanes to 1:1 methylene chloride-hexanes gradient elution). The initial product-containing fraction contained predominantly diiodinated material (by mass) with some monoiododinated material. The remaining fractions were concentrated in vacuo to afford the product as a light yellow oil (579 mg, 54%). The product was not dried under vacuum due to volatility.