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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2378570생성일: 2026년 10월 27일

Sodium hydride → Methyl 3-[3-nitro-4-(piperazin-1-yl)phenyl]acrylate

https://huagongshe.com/reaction/2378570

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Phosphonium, (2-methoxy-2-oxoethyl)triphenyl-, bromide (1:1)HCID 2733211—
반응물3-Nitro-4-(piperazin-1-yl)benzaldehydeHCID 60711115—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물Methyl 3-[3-nitro-4-(piperazin-1-yl)phenyl]acrylateHCID 6874114074.9%

반응 단계

A solution of methoxycarbonylmethyl(triphenyl)phosphonium bromide (1.1 g, TCI) in THF (12.5 ml) was added with sodium hydride (115 mg, WAKO) under ice cooling, warmed to room temperature, then added dropwise with a solution of 3-nitro-4-(piperazin-1-yl)benzaldehyde (550.6 mg, MAYB) in THF (12.5 ml), and stirred at the same temperature for 16.5 hours. The reaction mixture was poured into brine (40 ml), and extracted with ethyl acetate (100 ml). The organic layer was washed successively with saturated aqueous sodium hydrogencarbonate and saturated brine, and dried, and then the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography (hexane:ethyl acetate=5:1) to obtain the title compound (Intermediate Int. n-19, 511 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07470807B2
출처 데이터셋uspto-grants-2008_12
ORD IDord-ac5ac3ea6cf647ec801334b8c52e1dd3
출처 메모uspto-grants-2008_12