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HRID 854433Erstellt: 25. Oktober 2026

Formamide → N-((2,4-Difluorophenyl)(tosyl)methyl)formamide

https://huagongshe.com/reaction/854433

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormamideHCID 713—
EduktChlorotrimethylsilaneHCID 6397—
Eduktp-Toluenesulfinic acidHCID 10818—
Edukt2,4-DifluorobenzaldehydeHCID 73770—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelHexaneHCID 8058—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
ProduktN-((2,4-Difluorophenyl)(tosyl)methyl)formamideHCID 22236872—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To 2,4-difluorobenzaldehyde (1.42 g, 10.0 mmol) is added toluene (5.0 mL), acetonitrile (5.0 mL), formamide (0.993 mL, 25.0 mmol) and chlorotrimethylsilane (1.40 mL, 11.0 mmol) in order. The cloudy mixture is heated to 50° C. and stirred at this temperature for 7 hours. p-Toluenesulfinic acid (2.19 g, 14.0 mmol) is added, and the mixture stirred at 50° C. for 6 hours, then for 3 hours at room temperature. MTBE (18.0 mL) and water (17.0 mL) are added, and the mixture stirred at room temperature for 15 minutes. The layers are separated, and the aqueous layer extracted with MTBE (5.0 mL). Most of the solvents are removed from the combined organic extracts leaving a white semi-solid. To the residual is added hexane (10.0 mL) and water (10.0 mL), and the resulting slurry stirred at room temperature for 30 minutes, then filtered. The cake is washed with hexane (2×) and dried in a vacuum-oven (30° C.) for 18 hours. The title compound may be obtained as a white powder (2.58 g, 79%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07259171B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-65325c6b8ae64d94ac5499b682789c9c
Quellennotizuspto-grants-2007_08