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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279125생성일: 2026년 10월 26일

Methyl iodide → 2-(4-Chlorophenylsulfonyl)-3-(3-cyanophenylamino)-3-methylsulfanyl-2-propenenitrile

https://huagongshe.com/reaction/279125

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물3-Cyanophenyl isothiocyanateHCID 76578—
반응물2-(4-Chlorobenzenesulfonyl)acetonitrileHCID 735829—
용매AcetoneHCID 180—
생성물2-(4-Chlorophenylsulfonyl)-3-(3-cyanophenylamino)-3-methylsulfanyl-2-propenenitrileHCID 7015062896.2%

반응 단계

A solution of 4-chlorophenylsulfonylacetonitrile (1.0 g, 4.64 mmol) in dry acetone (10 ml) was stirred while dry potassium carbonate (1.28 g, 9.28 mmol) and 3-cyanophenyl isothiocyanate (0.78 g, 4.87 mmol) were added. The resulting mixture was stirred at room temperature under nitrogen for 20 h. Excess of potassium carbonate was filtered off, methyl iodide (0.859 ml, 13.9 mmol) was added to the filtrate, and stirring was continued for 3 h. The mixture was evaporated and the residue was dissolved in dichloromethane and extracted with water and brine. The organic phase was dried over magnesium sulphate, filtered and evaporated to afford 1.74 g (96%) of the title compound as golden brown crystals. Mp 168-170° C. 1H NMR (200 MHz, CDCl3): δ=2.22 (s, 3H), 7.50-7.68 (m, 6H), 7.84-7.93(m, 2H), 9.89 (br s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362205B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-402b08af9dbc43d7a51f29e05e70d838
출처 메모uspto-grants-2002_03