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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 369133Erstellt: 26. Oktober 2026

Hydrochloric Acid → 3,4-dibenzyloxy-5-(2-hydroxyethyl)-2(5H)-furanone

https://huagongshe.com/reaction/369133

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBenzyl BromideHCID 7498—
EduktDiisopropylethylamineHCID 81531—
Edukt3-benzyloxy-4-hydroxy-5-(2-hydroxyethyl)-2(5H)-furanoneHCID 54723596—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3,4-dibenzyloxy-5-(2-hydroxyethyl)-2(5H)-furanoneHCID 2118410660%

Reaktionsschritte

A mixture of 1.25 g (5 mmol) of 3-benzyloxy-4-hydroxy-5-(2-hydroxyethyl)-2(5H)-furanone, 15 mL of THF, 871 μL (5.0 mmol) of diisopropylethylamine and 631 μL (5.2 mmol) of benzyl bromide were combined under argon. The reaction mixture was warmed to reflux for 5 hours, and upon cooling, a suspension formed which was poured into 50 mL of 5% aqueous HCl solution and extracted with 100 mL of ether. The ether fraction was separated and sequentially washed with 30 mL of 5% aqueous HCl, 30 mL of H2O, 30 mL of saturated NAHCO3 solution, 30 mL of H2O, 30 mL of brine, dried (MgSO4) and concentrated to a colorless oil. Purification over silica gel using EtOAc/hexanes (2/3) provided 3,4-dibenzyloxy-5-(2-hydroxyethyl)-2(5H)-furanone as a faint pink colored oil (1.0 g, 60% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06136832
Quelldatensatzuspto-grants-2000_10
ORD IDord-f7de61ba73024918b77a3d4c202054eb
Quellennotizuspto-grants-2000_10