HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Glycine ethyl ester → N-Oleoylglycine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Glycine ethyl ester | HCID 12176 | — |
| Edukt | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Edukt | Glycinamide | HCID 69020 | — |
| Edukt | Oleic Acid | HCID 445639 | — |
| Edukt | Oleoyl Sarcosine | HCID 6912870 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | N-Oleoylglycine | HCID 6436908 | — |
Reaktionsschritte
N-Oleoyl glycine (FIG. 7) was prepared by coupling glycine ethyl ester to oleic acid with EDCI (Cravatt et al. (1996) J. Am. Chem. Soc. 118, 580-590; Patterson et al. (1996) J. Am. Chem. Soc. 118, 5938-5945) followed by sequential transformation to the carboxylic acid (LiOH) and glycinamide (EDCI, NH4OH;). N-Oleoyl sarcosine was purchased (Pfaltz and Bauer) and converted to its ethyl ester by coupling with EtOH (DCC).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06858649B1 |
| Quelldatensatz | uspto-grants-2005_02 |
| ORD ID | ord-f5ac59a7fb8540c8a6d0e1f04c8cecc0 |
| Quellennotiz | uspto-grants-2005_02 |