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HRID 279099作成日:2026年10月26日

Methyl iodide → 3-(3,5-Bis(trifluoromethyl)phenylamino)-2-methanesulfonyl-3-methylsulfanyl-2-propenenitrile

https://huagongshe.com/reaction/279099

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Potassium CarbonateHCID 11430—
反応物(Methylsulfonyl)acetonitrileHCID 75283—
反応物3,5-Bis(trifluoromethyl)phenyl isothiocyanateHCID 2733395—
溶媒AcetoneHCID 180—
生成物3-(3,5-Bis(trifluoromethyl)phenylamino)-2-methanesulfonyl-3-methylsulfanyl-2-propenenitrileHCID 7398658483.3%

反応手順

To a solution of methanesulfonylacetonitrile (0.55 g, 4.6 mmol) in dry acetone (10 ml) first dry potassium carbonate (1.28 g, 9.3 mmol) and then 3,5-bis(trifluoromethyl)phenyl isothiocyanate (1,32 g, 4.7 mmol) were added. The resulting mixture was stirred at room temperature under nitrogen for 4 h, and then filtered. To the filtrate methyl iodide (0.86 ml, 13.9 mmol) was added. The mixture was stirred at room temperature for 2 h. The reaction mixture was filtered and the filtrate was concentrated. The residue was dissolved in dichloromethane and washed with water. The organic layer was dried (sodium sulfate) and concentrated. The residue was recrystallised from ethyl acetate/heptane 1:2 to give the title compound (1.55 g, 83%). Mp 129-131° C. 1H NMR (200 MHz, CDCl3): δ=2.35 (s, 3H), 3.25 (s, 3H), 7.77 (s, 2H), 7.80 (s, 1H)H), 9.90 (br s, 1H); EI SP/MS: 404 (M+).

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-a5adb4c5eb6b4c8486c0ee56cbd5c63b
出典メモuspto-grants-2002_03