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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 616598생성일: 2026년 10월 24일

[[o-(Allyloxy)phenoxy]methyl]oxirane → 1-[3-(o-Allyloxy-phenoxy)-2-hydroxypropyl]-4-(2-oxo-hexahydro-1-pyrimidinyl)piperidine

https://huagongshe.com/ko/reaction/616598

반응식

참여 물질

역할이름HCID투입량
반응물[[o-(Allyloxy)phenoxy]methyl]oxiraneHCID 5743337—
반응물1-(Piperidin-4-yl)-1,3-diazinan-2-oneHCID 15572666—
용매EthanolHCID 702—
생성물1-[3-(o-Allyloxy-phenoxy)-2-hydroxypropyl]-4-(2-oxo-hexahydro-1-pyrimidinyl)piperidineHCID 20368036—

반응 단계

A solution of 10.3 g of 1-(o-allyloxy-phenoxy)-2,3-epoxy-propane and 9.15 g of 1-(4-piperidyl)-2-oxo-hexahydropyrimidine in 7 ml abs. ethanol is heated for 5 hours to 95° C and then evaporated in vacuo. The residue is recrystallised from isopropanol to yield the 1-[3-(o-allyloxy-phenoxy)-2-hydroxypropyl]-4-(2-oxo-hexahydro-1-pyrimidinyl)-piperidine, which melts at 122°-125° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04075208
출처 데이터셋uspto-grants-1978_02
ORD IDord-78a02935df9f4be98813576cff7f00fe
출처 메모uspto-grants-1978_02