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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279099생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/279099

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물(Methylsulfonyl)acetonitrileHCID 75283—
반응물3,5-Bis(trifluoromethyl)phenyl isothiocyanateHCID 2733395—
용매AcetoneHCID 180—
생성물3-(3,5-Bis(trifluoromethyl)phenylamino)-2-methanesulfonyl-3-methylsulfanyl-2-propenenitrileHCID 7398658483.3%

반응 단계

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+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362205B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-a5adb4c5eb6b4c8486c0ee56cbd5c63b
출처 메모uspto-grants-2002_03