L-Serine → L-Serine, methyl ester, hydrochloride (1:1)
Reaktionsgleichung
[C:1]([Cl:4])(=O)C.[NH2:5][C@H:6]([C:9]([OH:11])=[O:10])[CH2:7][OH:8]>CO>[ClH:4].[NH2:5][C@@H:6]([CH2:7][OH:8])[C:9]([O:11][CH3:1])=[O:10]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Methanol (450 mL) in a round-bottom flask was cooled to 0° C. and acetyl chloride (55 mL, 0.77 mol) was added dropwise. After completion of the addition, the mixture was stirred at ambient temperature for 10 min and H-Ser-OH (30 g, 0.29 mol) was added in three portions. The reaction mixture was heated at 80° C. for 2 h and then concentrated. The residue was dried under vacuum to afford (S)-methyl 2-amino-3-hydroxypropanoate hydrochloride (quantitative) as a colorless solid, which was used in the next step without further purification.
Aufarbeitung
- additionAfter completion of the addition
- temperatureThe reaction mixture was heated at 80° C. for 2 h
- concentrationconcentrated
- customThe residue was dried under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-0aa4fe0dd32d40968fc32e8b983d26a1
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09434761B2
Notizen zur Reaktion
Wird geladen…