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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30825생성일: 2026년 10월 24일

Triethylborane → 2-(2-Fluoro-5-nitrophenyl)-2-methylpent-4-enal

https://huagongshe.com/ko/reaction/30825

반응식

참여 물질

역할이름HCID투입량
반응물TriethylboraneHCID 7357—
반응물Allyl AlcoholHCID 7858—
반응물TriethylamineHCID 8471—
반응물TriphenylphosphineHCID 11776—
반응물Lithium ChlorideHCID 433294—
반응물2-(2-Fluoro-5-nitrophenyl)propanalHCID 86600438—
촉매palladium(II) acetateHCID 167845—
용매TetrahydrofuranHCID 8028—
용매Sodium BicarbonateHCID 516892—
생성물2-(2-Fluoro-5-nitrophenyl)-2-methylpent-4-enalHCID 86600439—

반응 단계

To a solution of palladium acetate (0.1 eq), triphenylphosphine (0.2 eq), lithium chloride (1.0 eq) in THF were sequentially added 2-(2-fluoro-5-nitrophenyl) propanal (1.1 eq) in THF, allyl alcohol (1.0 eq), triethylamine (1.2 eq) and triethylborane (2.4 eq) under nitrogen at room temperature. Solution was allowed to stir for 2 h. Mixture was diluted with saturated solution of sodium bicarbonate, extracted with ethyl acetate. Organics were washed with brine, dried with sodium sulfate and concentrated. Crude product was purified using flash chromatography (85% Hex: 15% EtoAc) on silica to afford 2-(2-fluoro-5-nitrophenyl)-2-methylpent-4-enal.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423150B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-c0ef632ba96748608141c61764770d25
출처 메모uspto-grants-2008_09