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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1670Erstellt: 23. Oktober 2026

Benzyl Bromide → Methyl 4-(benzyloxy)-2-hydroxybenzoate

https://huagongshe.com/de/reaction/1670

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
EduktMethyl 2,4-DihydroxybenzoateHCID 16523—
LösungsmittelAcetoneHCID 180—
ProduktMethyl 4-(benzyloxy)-2-hydroxybenzoateHCID 225489—

Reaktionsschritte

To a stirred, 0° C. solution of methyl 2,4-dihydroxybenzoate (50 g, 300 mmol) in acetone (1000 mL) was added K2CO3 (150 g, 1000 mmol) and benzyl bromide (330 mmol, 39 mL). The solution was allowed to warm to ambient temperature over 48 h. The reaction solution was filtered through celite and the acetone solution stripped down under reduced pressure. The crude oil was dissolved in EtOAc (1000 mL) and washed with water (250 mL), and saturated aqueous NaHCO3 (500 mL). The EtOAc layer was dried (MgSO4), filtered, and the EtOAc was removed under reduced pressure. The crude product was purified by pressurized silica gel column chromatography using 5:1 hexanes:EtOAc. Evaporation of the hexanes:EtOAc mixture gave the desired methyl 4-benzyloxy-2-hydroxybenzoate as a white powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726172
Quelldatensatzuspto-grants-1998_03
ORD IDord-b4fd402e735143d2ba1df2c8a9a0fe8f
Quellennotizuspto-grants-1998_03