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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256179생성일: 2026년 10월 26일

Piperidine → 2-(2-Nitro-5-piperdinylphenyl)-1,3-dioxolane

https://huagongshe.com/reaction/256179

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물2-(5-Chloro-2-nitrophenyl)-1,3-dioxolaneHCID 267385—
생성물2-(2-Nitro-5-piperdinylphenyl)-1,3-dioxolaneHCID 13987598100%

반응 단계

A mixture of 2-(5-chloro-2-nitrophenyl)-1,3-dioxolane (21.3 g, 0.09 mole) and piperidine (39.6 g, 0.46 mole) was heated at reflux in an oil bath. After 3 hours, excess piperidine was evaporated and the residue partitioned between water and dichloromethane. The organic phase was separated and the aqueous layer extracted with dichloromethane. Combined extracts were washed with water, dried over magnesium sulfate and concentrated in vacuo to afford 2-(2-nitro-5-piperdinylphenyl)-1,3-dioxolane (21.6 g, 100%) as a dark colored oil which was used without further purification. An analytical sample was purified by flash chromatography using dichloromethane as eluant to give a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04701459
출처 데이터셋uspto-grants-1987_10
ORD IDord-780747b03da34d5da4302f7cf0abbebe
출처 메모uspto-grants-1987_10