Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trimethylamine | HCID 1146 | — |
| Edukt | 4-Chloro-3-hydroxybutyric acid ethyl ester, (3R)- | HCID 2734445 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | (-)-Carnitine | HCID 10917 | 71% |
Reaktionsschritte
110 g of ethyl (+) (R)-4-chloro-3-hydroxybutyrate, prepared according to Example 2, and 280 ml of 45% trimethylamine in H2O are placed in a 0.6-liter reactor. The reaction mixture is heated to 80° C. and kept at this temperature for 2 h. After cooling and removing the excess of trimethylamine, the aqueous solution is extracted with 0.5 l of methylene chloride and analyzed with HPLC. L-carnitine is obtained with 71% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06566552B2 |
|---|
| Quelldatensatz | uspto-grants-2003_05 |
|---|
| ORD ID | ord-30cb55472c544eebb4548c4d9e4addaf |
|---|
| Quellennotiz | uspto-grants-2003_05 |
|---|
