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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 987937Erstellt: 24. Oktober 2026

Sodium hydride → 2-tert-Butoxycarbonylamino-3-(4-fluoro-phenylsulfanyl)-propionic Acid Methyl Ester

https://huagongshe.com/de/reaction/987937

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt4-FluorothiophenolHCID 67789—
Edukt2-Tert-butoxycarbonylamino-3-(toluene-4-sulfonyloxy)-propionic acid methyl esterHCID 2818162—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-tert-Butoxycarbonylamino-3-(4-fluoro-phenylsulfanyl)-propionic Acid Methyl EsterHCID 69853553—

Reaktionsschritte

A stirred solution of 4-fluorothiophenol (1.24 g, 9.65 mmol) in N,N-dimethyl formamide (10 ml) was treated with sodium hydride (240 mg, 9.37 mmol) and the reaction mixture was stirred at room temperature for 30 minutes. 2-tert-Butoxycarbonylamino-3-(toluene-4-sulfonyloxy)-propionic acid methyl ester (3 g, 8.04 mmol) in N,N dimethyl formamide (ml) was added, the resulting mixture was stirred for two hours and then concentrated in vacuo. The residue was dissolved in ethyl acetate (100 ml) and washed with water (2*80 ml) and brine. The organic layer was dried (anhydrous magnesium sulfate) and concentrated in vacuo to give, after purification by flash chromatography on silica gel, 2-tert-butoxycarbonylamino-3-(4-fluoro-phenylsulfanyl)-propionic acid methyl ester (2.28 g, 83%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06632826B1
Quelldatensatzuspto-grants-2003_10
ORD IDord-b64c81fbdb9f4444baef37d83817bdde
Quellennotizuspto-grants-2003_10