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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1759609Erstellt: 25. Oktober 2026

Methanol → Methyl (2S)-2-amino-3-(4-fluorophenyl)propanoate

https://huagongshe.com/reaction/1759609

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktThionyl ChlorideHCID 24386—
Edukt4-fluoro-L-phenylalanineHCID 716312—
ProduktMethyl (2S)-2-amino-3-(4-fluorophenyl)propanoateHCID 7018988—

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

1.8 g (10 mmole) of 4-fluorophenylalanine is suspended in 3.0 ml of methanol and cooled to -10° C. under nitrogen and 0.81 ml of thionylchloride added dropwise, keeping the temperature at or below -2° C., and stirred for 1 hour at -5° C. to -10° C. About 10 ml of methanol was added and the solution stirred at room temperature overnight. The solution was concentrated in vacuo and the residue triturated with dry ether and filtered to give the hydrochloride salt of 4-fluorophenylalanine methyl ester, m.p. 177.5° to 178° C. The ester hydrochloride is substituted for L-phenylalanine methyl ester hydrochloride in the procedure of Example 6a to yield 6b.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04341698
Quelldatensatzuspto-grants-1982_07
ORD IDord-dca3d7ddc0b54f67a1d51838bcc3276e
Quellennotizuspto-grants-1982_07