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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610592Generated: October 31, 2026

Benzyl 4-Hydroxybenzoate → HCID 22261396, compound

https://huagongshe.com/reaction/1610592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-HydroxybenzoateHCID 7180—
Reactant2-BromopyridineHCID 7973—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
ProductHCID 22261396HCID 22261396—

Reaction Steps

To a solution of benzyl 4-hydroxybenzoate (25.3 g, 111 mmol) in N,N-dimethylformamide (60 ml) was added potassium tert-butoxide (12.4 g, 111 mmol), and the mixture was stirred at room temperature for 1 hr. The reaction solution was evaporated under reduced pressure and 2-bromopyridine (24.5 g, 155 mmol), a copper powder (1.76 g, 27.7 mmol) and N,N-imethylformamide (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). Recrystallization from ethyl acetate-hexane gave the objective substance (25.5 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-7b824920d969412eaad66c3e3c286d1b
Source noteuspto-grants-2006_01