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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1633211생성일: 2026년 10월 25일

Sodium hydride → Diethyl 2-fluoro-2-phenylmalonate

https://huagongshe.com/reaction/1633211

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Diethyl phenylmalonateHCID 66514—
반응물N-fluoro-N-neopentyl-n-butylsulfonamideHCID 13222564—
반응물HCID 178418361HCID 178418361—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물Diethyl 2-fluoro-2-phenylmalonateHCID 424664266.6%

반응 단계

Diethyl phenylmalonate (708 mg, 650 μL, 3 mmole) was dissolved in anhydrous tetrahydrofuran (5 mL) under nitrogen. Sodium hydride (144 mg as a 60% oil dispersion, 3.6 mmole) was added and the mixture was stirred until hydrogen evolution ceased (about 15 minutes). The solution was then diluted with anhydrous toluene (10 mL) and added dropwise to a solution of N-fluoro-N-neopentyl-n-butylsulfonamide (675 mg, 3 mmole) in anhydrous toluene (5 mL) and the mixture was stirred at room temperature under nitrogen. After 30 minutes the reaction mixture was diluted with ether (100 mL), washed with aqueous 1N oxalic acid (30 mL), 10% aqueous potassium bicarbonate (30 mL), and saturated aqueous sodium chloride (30 mL) solutions, and then dried over anhydrous magnesium sulfate. Filtration, removal of solvent under reduced pressure, and purification by flash column chromatography (silica, 1:1 methylene chloride-hexane) yielded diethyl 2-fluoro-2-phenylmalonate as a colorless liquid (508 mg). 1H NMR was consistent with the desired structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04479901
출처 데이터셋uspto-grants-1984_10
ORD IDord-dbbcb9f26df64ca7bb35c3fdc0a55e86
출처 메모uspto-grants-1984_10