HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → Palmitoylethanolamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Hexadecanoic acid, ethenyl ester | HCID 69658 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Product | Palmitoylethanolamide | HCID 4671 | — |
Reaction Steps
In an exemplary embodiment, 20 mmol ethanolamine was reacted with 1 mmol vinyl stearate at 80° C. for 1 hour in the presence of 1% sodium methoxide. N-stearoylethanolamine with 96% purity was obtained after the removal of excess ethanolamine without further purification. In another exemplary embodiment, 20 mmol ethanolamine was reacted with 1 mmol vinyl palmitate at 60° C. for 1.5 hours in the presence of 1% sodium methoxide. N-palmitoylethanolamine with 98% purity was obtained after the removal of excess ethanolamine without further purification. More examples of reacting the alkanolamine and the vinyl ester of the fatty acid to prepare the high-purity fatty acid N-acylalkanolamine in a high yield are described in Examples 1-8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221747B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-87077d1c2c5f4de8b2fbb1eea084ec2f |
| Source note | uspto-grants-2015_12 |