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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 888336생성일: 2026년 10월 26일

Hydrochloric Acid → 6,6,6-Trifluoro-2-methyl-2-(3,3,3-trifluoropropylsulfonyl)-4-hexenenitrile

https://huagongshe.com/reaction/888336

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물4,4,4-Trifluoro-2-butenyl p-toluenesulfonateHCID 53655839—
반응물2-(3,3,3-Trifluoropropylsulfonyl)propionitrileHCID 57788363—
생성물6,6,6-Trifluoro-2-methyl-2-(3,3,3-trifluoropropylsulfonyl)-4-hexenenitrileHCID 72281791—

반응 단계

To a solution of 1.5 g of 4,4,4-trifluoro-2-butenyl p-toluenesulfonate and 1.2 g of 2-(3,3,3-trifluoropropylsulfonyl)propionitrile in 30 ml of tetrahydrofuran was added 0.2 g of sodium hydride (60% in oil) at room temperature. The reaction mixture was stirred at the same temperature for 2 days. To the reaction mixture was added 10% hydrochloric acid and then extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography to obtain 0.80 g of 6,6,6-trifluoro-2-methyl-2-(3,3,3-trifluoropropylsulfonyl)-4-hexenenitrile (hereinafter referred to as the present compound (34)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08247595B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-4fb3e7227b194dea95a8f344ba55403c
출처 메모uspto-grants-2012_08