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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 749598생성일: 2026년 10월 25일

Hydrochloric Acid → (4-(Trifluoromethyl)benzyl)malononitrile

https://huagongshe.com/reaction/749598

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물(4-(Trifluoromethyl)benzylidene)malononitrileHCID 714296—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
생성물(4-(Trifluoromethyl)benzyl)malononitrileHCID 1065674351.3%

반응 단계

First, 4.44 g of (4-(trifluoromethyl)benzylidene)malononitrile was dissolved in 20 ml of ethanol, and while stirring at room temperature, a suspension of 0.19 g of sodium borohydride in 5 ml of ethanol was added dropwise, followed by stirring at room temperature for 30 minutes. Then, 10% hydrochloride acid was added to the reaction mixture, which became acidic and was extracted with diethyl ether. The organic layer was successively washed with 10% hydrochloric acid, a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 2.30 g of (4-(trifluoromethyl)benzyl)malononitrile (the intermediate (4)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07402691B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-d8439fc2695e4fb0b52aae099c3403eb
출처 메모uspto-grants-2008_07