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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885090Generated: October 25, 2026

Docosanedioic acid → 9,10-Epoxy-18-hydroxyoctadecanoic acid

https://huagongshe.com/reaction/1885090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDocosanedioic acidHCID 244872—
Reactant18-Hydroxy-9-octadecenoic acidHCID 3014191—
Reactant22-Hydroxydocosanoic acidHCID 5282922—
Reactant9,10,18-Trihydroxystearic acidHCID 5282938—
Reactant9,16-Dihydroxyhexadecanoic acidHCID 14259006—
Reactant9-Octadecenedioic acidHCID 25202007—
Product9,10-Epoxy-18-hydroxyoctadecanoic acidHCID 9818312—

Reaction Steps

The present invention provides a process for isolating, from outer birch bark, at least one of 9,10-epoxy- 18-hydroxyoctadecanoic acid; 9,16-dihydroxyhexadecanoic acid; 9,10,18-trihydroxyoctadecanoic acid (phloionolic acid); 20-hydroxyeicasanoic acid; 22-hydroxydocosanoic acid; 18-hydroxyoctadec-9-enoic acid; docosandioic acid; and octadec-9-enedioic acid; comprising: (1) subjecting the outer birch bark to hydrolysis to provide a second outer birch bark and a second solution; (2) separating the second solution from the second outer birch bark; (3) condensing the second solution at a temperature below about 50° C. to provide at least one of 9,10-epoxy-18-hydroxyoctadecanoic acid; 9,16-dihydroxyhexadecanoic acid; 9,10,18-trihydroxyoctadecanoic acid (phloionolic acid); 20-hydroxyeicasanoic acid; 22-hydroxydocosanoic acid; 18-hydroxyoctadec-9-enoic acid; docosandioic acid; and octadec-9-enedioic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06768016B2
Source datasetuspto-grants-2004_07
ORD IDord-56a06ae7faae48a798ff3713627a1750
Source noteuspto-grants-2004_07