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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1610600Erstellt: 26. Oktober 2026

Benzyl 4-Hydroxybenzoate → Benzyl 4-(pyridin-3-yloxy)benzoate

https://huagongshe.com/reaction/1610600

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl 4-HydroxybenzoateHCID 7180—
Edukt3-BromopyridineHCID 12286—
EduktPotassium tert-butoxideHCID 23665647—
KatalysatorCopperHCID 23978—
LösungsmittelDimethylformamideHCID 6228—
ProduktBenzyl 4-(pyridin-3-yloxy)benzoateHCID 22262109—

Reaktionsschritte

To a solution of benzyl 4-hydroxybenzoate (25.0 g, 110 mmol) in N,N-dimethylformamide (60 ml) was added potassium tert-butoxide (12.3 g, 110 mmol), and the mixture was stirred at room temperature for 1 hr. The reaction solution was evaporated under reduced pressure, and 3-bromopyridine (25.0 g, 110 mmol), a copper powder (1.76 g, 27.2 mmol) and N,N-dimethylformamide (80 ml) were added. The mixture was stirred at 120° C. for 8 hrs. The reaction solution was filtered with celite and the filtrate was evaporated under reduced pressure. To the residue was added water (500 ml) and the mixture was extracted with ethyl acetate (500 ml). The extract was washed successively with water and saturated brine, dried (anhydrous magnesium sulfate) and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1-2:1) to give the objective substance (18.0 g, 54%, crude).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06982348B2
Quelldatensatzuspto-grants-2006_01
ORD IDord-3fadcb0b6113453aac7fa19ac40d1eab
Quellennotizuspto-grants-2006_01