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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 614834생성일: 2026년 10월 26일

4-(Phenoxymethyl)piperidine → 2-Amino-1-[2-hydroxy-3-(4-phenoxymethylpiperidino)-propoxy]-3-nitrobenzene

https://huagongshe.com/reaction/614834

반응식

참여 물질

역할이름HCID투입량
반응물4-(Phenoxymethyl)piperidineHCID 3017444—
반응물1-(2-Amino-3-nitrophenoxy)-2,3-epoxypropaneHCID 11344838—
용매EthanolHCID 702—
생성물2-Amino-1-[2-hydroxy-3-(4-phenoxymethylpiperidino)-propoxy]-3-nitrobenzeneHCID 21327312—

반응 단계

A mixture of 40.0 g. 1-(2-amino-3-nitrophenoxy)-2,3-epoxypropane, 36.2 g. 4-phenoxymethylpiperidine and 450 ml. ethanol is stirred for 18 hours at ambient temperature and the solution thereby obtained of 2-amino-1-[2-hydroxy-3-(4-phenoxymethylpiperidino)-propoxy]-3-nitrobenzene (m.p. 117°-118° C.) is subsequently hydrogenated at ambient temperature in the presence of 1.0 g. platinum oxide. After filtration, the filtrate obtained is acidified with dilute hydrochloric acid, evaporated and the evaporation residue redissolved in ethanol/ethyl acetate. There are obtained 72.3 g. 2,3-diamino-1-[2-hydroxy-3-(4-phenoxymethylpiperidino)-propoxy]-benzene trihydrochloride (81% of theory) in the form of an amorphous substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04146630
출처 데이터셋uspto-grants-1979_03
ORD IDord-1c919157d63b4789acda1d6d8b1b2d84
출처 메모uspto-grants-1979_03