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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1972323Erstellt: 26. Oktober 2026

Benzyl Bromide → (S)-benzyl 2-(dibenzylamino)pentanoate

https://huagongshe.com/reaction/1972323

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
EduktSodium HydroxideHCID 14798—
EduktL-NorvalineHCID 65098—
LösungsmittelWaterHCID 962—
Produkt(S)-benzyl 2-(dibenzylamino)pentanoateHCID 44223288132,9%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Sodium hydroxide (0.513 Kg; 12.82 moles) and potassium carbonate (1.77 Kg, 12.82 moles) were dissolved in water (7.5 L) and cooled to 0° C. The resulting solution was treated with (S)-2-aminopentanoic acid (L-norvaline, 0.75 Kg; 6.41 moles) slowly at between 0-5° C. The stirred suspension was heated at 90° C. and benzyl bromide (4.385 Kg, 25.64 moles) was added dropwise. Heating was continued for a further 12 hours at 90° C. The reaction mixture was then cooled to ambient temperature, and extracted with ethyl acetate (2×6 liters). The layers were separated and the aqueous phase extracted twice with ethyl acetate. The combined organic extracts were dried over sodium sulfate, and the solvent removed under reduced pressure to obtain 3.3 Kg of crude (S)-benzyl 2-(dibenzylamino)pentanoate, a compound of formula (3), as a brown oil. This material was used in the next reaction without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08431733B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-f7b38c2c6f8f4157bf7f2030d294d5a7
Quellennotizuspto-grants-2013_04