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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279128생성일: 2026년 10월 26일

Acetone → 3-(3,5-Bis(trifluoromethyl)phenylamino)-2-isopropylsulfonyl-3-methylsulfanyl-2-propenenitrile

https://huagongshe.com/reaction/279128

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물2-(Propane-1-sulfonyl)acetonitrileHCID 519441—
반응물3,5-Bis(trifluoromethyl)phenyl isothiocyanateHCID 2733395—
생성물3-(3,5-Bis(trifluoromethyl)phenylamino)-2-isopropylsulfonyl-3-methylsulfanyl-2-propenenitrileHCID 8658373999%

반응 단계

A solution of 2-propanesulphonylacetonitrile (4.0 g, 27.2 mmol) in dry acetone (50 ml) was stirred while dry potassium carbonate (7.52 g, 54.4 mmol) and 3,5-bis(trifluoromethyl)phenyl isothiocyanate (7.72 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 (5.08 ml, 81.6 mmol) was added to the filtrate, and stirring was continued for 48 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 11.65 g (99%) of the title compound as yellowish brown crystals. Mp 130-133° C.1H NMR (200 MHz, CDCl3): δ=1.47 (d, 6H), 2.35 (s, 3H), 3.44 (heptet, 1H), 7.73 (s, 2H), 7.80 (s, 1H), 10.10 (br s, 1H);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362205B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-5eebe8b707cb4261be0e869ad8d31568
출처 메모uspto-grants-2002_03