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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610585Generated: November 2, 2026

Methanol → 2-Methyl-5-phenoxypyridine

https://huagongshe.com/reaction/1610585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBromobenzeneHCID 7961—
Reactant2-Methyl-5-hydroxypyridineHCID 14275—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
Product2-Methyl-5-phenoxypyridineHCID 12673497—

Reaction Steps

To a solution of 6-methylpyridin-3-ol (25.2 g, 231 mmol) in N,N-dimethylformamide (100 ml) was added potassium tert-butoxide (25.9 g, 231 mmol), and the mixture was stirred at room temperature for 1 hr. The reaction solution was evaporated under reduced pressure and diluted with N,N-dimethylformamide (100 ml). A copper powder (3.7 g, 58 mmol) and bromobenzene (36.3 g, 231 mmol) were added, and the mixture was stirred at 120° C. overnight. Methanol was added to the reaction solution and insoluble material was filtered off using celite. The filtrate was diluted with water (500 ml) and the mixture was extracted with ethyl acetate (500 ml×2). 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=4:1) to give the objective substance (31 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-830997d5bae4401a860bf652c9124cef
Source noteuspto-grants-2006_01