HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 267310Erstellt: 26. Oktober 2026
Hydrochloric Acid → Methyl 3-phenyl-DL-alaninate hydrochloride
https://huagongshe.com/reaction/267310
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | (R)-Methyl 2-amino-3-phenylpropanoate | HCID 853474 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Methyl 3-phenyl-DL-alaninate hydrochloride | HCID 3084017 | — |
Reaktionsschritte
5.0 Parts of D-phenylalanine methyl ester, dissolved in 80 parts of methanol, is treated, at room temperature, with 0.90 part of sodium methoxide. The mixture is heated rapidly to reflux and maintained at reflux for about 21/21/2 hours. Then the reaction mixture is cooled, acidified to pH 2 with concentrated hydrochloric acid and evaporated to dryness. The remaining crystalline residue is taken up in water, and sodium carbonate is added. 1,2-Dichloroethane is added to form two phases and the mixture is shaken and filtered. The organic layer is separated, washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate and filtered. The filtrate is acidified with hydrochloric acid, cooled and stripped of solvent. Trituration with ether of the material which remains after solvent removal and subsequent filtration yields DL-phenylalanine methyl ester hydrochloride, melting at about 162°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US03941831 |
|---|
| Quelldatensatz | uspto-grants-1976_03 |
|---|
| ORD ID | ord-f6450bc73f6049849051b7b04e4be03a |
|---|
| Quellennotiz | uspto-grants-1976_03 |
|---|