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HRID 279087作成日:2026年10月27日

Hydrochloric Acid → 3-(3,5-Bis(trifluoromethyl)phenylamino)-2-(4-chlorophenylsulfonyl)-3-methylsulfanyl-2-propenenitrile

https://huagongshe.com/reaction/279087

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Methyl iodideHCID 6328—
反応物Potassium CarbonateHCID 11430—
反応物Sodium BicarbonateHCID 516892—
反応物2-(4-Chlorobenzenesulfonyl)acetonitrileHCID 735829—
反応物3,5-Bis(trifluoromethyl)phenyl isothiocyanateHCID 2733395—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物3-(3,5-Bis(trifluoromethyl)phenylamino)-2-(4-chlorophenylsulfonyl)-3-methylsulfanyl-2-propenenitrileHCID 8658373193.6%

反応手順

To a solution of 4-chlorophenylsulfonylacetonitrile (1.10 g, 5.10 mmol) in dry acetone (12 ml) first dry potassium carbonate (1.41 g, 10.2 mmol) and then 3,5-bis(trifluoromethyl)phenyl isothiocyanate (1,44 g, 5.31 mmol) were added. The resulting mixture was stirred at room temperature under nitrogen for 1 h, and then filtered. To the filtrate a solution of sodium hydrogencarbonate (0.86 g) in water (15 ml) and methyl iodide (0.945 ml, 15.3 mmol) was added. The mixture was stirred at room temperature for 3.5 h. Then pH was adjusted to ˜4 with 1N HCl. The precipitate was filtered off and washed with water to give 2.39 g (93%) of the title compound. Recrystallisation could be done from ethyl acetate/heptane 1:3. Mp 150.5-152.5° C. 1H NMR (300 MHz, CDCl3): δ=2.25 (s, 3H), 7.57 (d, 2H), 7.79 (s, 2H), 7.83 (s, 1H), 7.88 (d, 2H), 10.0 (br s, 1H); MA calc for C18H11ClF6N2O2S2: C, 43.17%; H, 2.21%; N, 5.59%. Found: C, 43.25%; H, 2.16%; N, 5.59%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06362205B1
出典データセットuspto-grants-2002_03
ORD IDord-fad4d7cfa295418ca915b590471dc9be
出典メモuspto-grants-2002_03