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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616685Generated: October 25, 2026

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

https://huagongshe.com/reaction/616685

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[[o-(Allyloxy)phenoxy]methyl]oxiraneHCID 5743337—
Reactant1-(Piperidin-4-yl)-1,3-diazinan-2-oneHCID 15572666—
SolventEthanolHCID 702—
Product1-[3-(o-Allyloxy-phenoxy)-2-hydroxypropyl]-4-(2-oxo-hexahydro-1-pyrimidinyl)piperidineHCID 20368036—

Reaction Steps

A solution of 10.3 g of 1-(o-allyloxy-phenoxy)-2,3-epoxy-propane and 9.15 g of 1-(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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04075335
Source datasetuspto-grants-1978_02
ORD IDord-a35610d8840f4c2bbe4e9ff9f35cabf7
Source noteuspto-grants-1978_02