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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 844830Erstellt: 24. Oktober 2026

(S)-(-)-N-Benzyl-1-phenylethylamine → (S)-3-[2-(4-Acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic Acid (S)-N-Benzyl-alpha-methylbenzylamine Salt

https://huagongshe.com/de/reaction/844830

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(S)-(-)-N-Benzyl-1-phenylethylamineHCID 1268085—
Edukt(+/-)-3-[2-(4-Acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic acidHCID 9827476—
LösungsmittelEthanolHCID 702—
Produkt(S)-3-[2-(4-Acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic Acid (S)-N-Benzyl-alpha-methylbenzylamine SaltHCID 8675801343%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

Ethanol (125 g) was added to (+/−)-3-[2-(4-acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic acid (11a, 25 g, 85 mmol) and the resulting solution stirred at 20° C. (S)-N-Benzyl-α-methylbenzylamine (21, 22.5 g, 106 mmol) was added to the solution and the resulting mixture allowed to stir at 20° C. for 23 hours. The mixture was filtered and the product washed with ethanol (10 mL) and vacuum dried at ambient temperature to give (S)-3-[2-(4-acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic acid (S)-N-benzyl-α-methylbenzylamine salt (22a): 18.6 g (36.8 mmol, 43% yield or 86% of theory); Chiral assay (HPLC): 99.2 area % (S) isomer 23a; mp: 152-154° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06380400B1
Quelldatensatzuspto-grants-2002_04
ORD IDord-a06b05bdbbdc43fe9632c2941295f96a
Quellennotizuspto-grants-2002_04