Methanol → L-cysteic acid methyl ester hydrochloride

HRID 332609

Reaktionsgleichung

Reaktionsgleichung von HRID 332609
[NH2:1][C@H:2]([C:8]([OH:10])=[O:9])[CH2:3][S:4](=[O:7])([OH:6])=[O:5].S(Cl)([Cl:13])=O.[CH3:15]O>>[ClH:13].[CH3:15][O:9][C:8](=[O:10])[C@H:2]([CH2:3][S:4](=[O:6])([OH:7])=[O:5])[NH2:1]

Komponenten

4

Edukt 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 72886L-Cysteic acid

Produkt 1

HCID 86673321L-cysteic acid methyl ester hydrochlorideAusbeute 75 %

Versuchsvorschrift

L-cysteic acid (300 mg, 1.77 mmol) was dissolved in methanol (12 mL), and thionyl chloride (2.5 mL, 34 mmol) was slowly added at 0° C. After stirring at room temperature overnight, the reaction mixture was concentrated under reduced pressure, and the obtained residue was suspended in diisopropyl ether. The suspension was filtered to give the title compound as white crystals (291 mg, 1.33 mmol, 75%).

Aufarbeitung

  1. concentrationthe reaction mixture was concentrated under reduced pressure
  2. filtrationThe suspension was filtered

Quellen und Nachweise

ORD-Eintrag
ord-2050740cabfa4238933a646dca392ceb
Quelldatensatz
uspto-grants-2014_11
Patentnummer
US08877805B2

Verknüpfte Notizen

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