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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25681Erstellt: 25. Oktober 2026

Triethylamine → tert-butyl (S)-(2-hydroxy-1-phenyl-ethylamino)-acetate

https://huagongshe.com/reaction/25681

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktAmmonium ChlorideHCID 25517—
Edukttert-Butyl bromoacetateHCID 79177—
Edukt2-Amino-2-phenylethan-1-olHCID 134797—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-butyl (S)-(2-hydroxy-1-phenyl-ethylamino)-acetateHCID 5906586933%

Reaktionsschritte

Following the literature procedure (Panek, J., J. Org. Chem., 1998, 63, 2382), triethylamine (6.2 ml, 44.5 mmole) was added to a solution of (S)-phenylglycinol (5 g, 36.45 mmole) in anhydrous tetrahydrofuran (150 ml) under argon at 0° C. After stirring for 15 min, tert-butyl bromoacetate (5.9 ml, 39.96 mmole) was added slowly to this cooled solution. The resulting mixture was warmed to room temperature, and stirred for 15 h. Saturated ammonium chloride aqueous solution was added, and the aqueous layer was extracted with diethyl ether (3 times). The combined extracts were washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to dryness in vacuo. The resulting solid was recrystallized from a diethyl ether/n-hexane mixture to give tert-butyl (S)-(2-Hydroxy-1-phenyl-ethylamino)-acetate as a white solid (3 g, 33%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858591B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-4155ccae976a4f078fbd239bf2b9a877
Quellennotizuspto-grants-2005_02