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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074457Generated: October 27, 2026

Epichlorohydrin → HCID 20496759, compound

https://huagongshe.com/reaction/1074457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantPiperidineHCID 8082—
Reactant3-Phenylchroman-7-olHCID 20496761—
ProductHCID 20496759HCID 20496759—

Reaction Steps

17 g 7-hydroxy-3-phenyl-3,4-dihydro-2H-1-benzopyrane, 0.1 cm3 piperidine and 100 cm3 1-chloro-2,3-epoxypropane were stirred for 6 hours at a temperature of 90° C. The solution was evaporated under reduced pressure, the residue was dissolved in 150 cm3 benzene and the obtained solution was extracted twice with 25--25 cm3 saturated sodium carbonate solution. The benzene phase was separated from the precipitated resin, clarificated with charcoal, filtered and evaporated. Crystallizing the residue from methanol, 15 g pure crystalline 1,2-epoxy-3-(3-phenyl-3,4-dihydro-2H-1-benzopyrane-7-yloxy)-propane was obtained (m.p. 117°-119° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04391821
Source datasetuspto-grants-1983_07
ORD IDord-e2d1ffefd2ad4a80a2193f334e7eb777
Source noteuspto-grants-1983_07