HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → Oleoylethanolamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Oleic Acid | HCID 445639 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Oleoylethanolamide | HCID 5283454 | — |
Reaction Steps
In an exemplary embodiment, 1 mmol oleic acid was reacted with 1 mmol ethanolamine in 1.5 mL hexane at 65° C. for 3 hours in the presence 30% lipase and 10 μL water. N-oleoyl ethanolamine with 96.6% purity was obtained and all oleic acid was consumed. In another exemplary embodiment, when the synthesis was conducted on a large scale (50 mmol of each of the reactants), the purity of N-oleoyl ethanolamine after crystallization purification was 96.1%. More examples of reacting the alkanolamine and the fatty acid to prepare the high-purity fatty acid N-acylalkanolamine in a high yield are described in Examples 9-18.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221747B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-188c955b7a494963abaf2054fb0d2e2f |
| Source note | uspto-grants-2015_12 |