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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233672Erstellt: 24. Oktober 2026

Benzyl Bromide → D-leucic acid benzyl ester

https://huagongshe.com/de/reaction/233672

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktTetrahydrofuranHCID 8028—
Edukt(R)-2-hydroxy-4-methylpentanoic acidHCID 439960—
LösungsmittelTriethylamineHCID 8471—
ProduktD-leucic acid benzyl esterHCID 9991100—

Reaktionsschritte

To 150 ml of tetrahydrofurane of 14.50 of D-leucic acid, 15.2 g of triethylamine and then 14.4 ml of benzyl bromide are added, and the solution was stirred for 3 hours while refluxing. The insoluble matter produced from the reaction solution was filtered off, and the filtrate was concentrated in vacuo. The obtained residue was dissolved and extracted in 150 ml of ethyl acetate. The ethyl acetate layer was washed twice with saturated bicarbonate water, twice with 1N hydrochloric acid, and twice with saturated brine sequentially, and dried over sodium sulfate anhydride, and concentrated in vacuo. The obtained oily residue was dried, and the captioned compound was obtained. Yield: 18.34 g.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05594006
Quelldatensatzuspto-grants-1997_01
ORD IDord-ec3d3fd529934f85b7a05b26f0e52b1d
Quellennotizuspto-grants-1997_01