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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1187795Erstellt: 26. Oktober 2026

Acetic Acid → 4-[(S)-1-(4-Bromo-phenyl)-ethylamino]-1-methoxy-2-phenyl-butan-2-ol

https://huagongshe.com/reaction/1187795

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt(alphaS)-4-Bromo-alpha-methylbenzenemethanamineHCID 852999—
Edukt3-Hydroxy-4-methoxy-3-phenyl-butyraldehydeHCID 59635677—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-[(S)-1-(4-Bromo-phenyl)-ethylamino]-1-methoxy-2-phenyl-butan-2-olHCID 59635799—

Reaktionsschritte

(S)-1-(4-Bromo-phenyl)-ethylamine (0.93 g), NaB(OAc)3 (0.98 g), and acetic acid (0.27 mL) were added in the given order to a solution of 3-hydroxy-4-methoxy-3-phenyl-butyraldehyde (0.90 g) in tetrahydrofuran (20 mL) at ca. 10-15° C. The cooling bath was removed and the mixture was stirred at room temperature for 2 h. Then, water (50 mL) and 1 M aqueous NaOH solution (20 mL) were added and the resulting mixture was stirred for another 30 min. The mixture was extracted with ethyl acetate and the combined extracts were washed with water and brine. After drying (MgSO4), the solvent was removed to give the title compound which was submitted to the subsequent reaction step without further purification. Yield: 1.80 g (quantitative).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08673899B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-cb55549e13d645ecb216ea5e0f73b3ab
Quellennotizuspto-grants-2014_03