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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073516Generated: November 2, 2026

2-Methylpyridine → 2-[3-(4-Phenoxyphenoxy)propyl]pyridine

https://huagongshe.com/reaction/1073516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpyridineHCID 7975—
Reactant1-(2-Bromoethoxy)-4-phenoxybenzeneHCID 13254487—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-[3-(4-Phenoxyphenoxy)propyl]pyridineHCID 1415443952.4%

Reaction Conditions

Temperature-50 °C

Reaction Steps

To a solution of α-picoline (1.0 g, 11 mmol) in dry tetrahydrofuran (20 ml), n-butyl lithium (8 ml, 11 mmol; 1.4 mmol/ml) was added at -50° C. under nitrogen stream until the reaction mixture turned red. After stirring at -50° C. for 30 minutes, 2-(4-phenoxyphenoxy)ethyl bromide (3.0 g, 10 mmol) was dropwise added thereto at -50° C., and stirring was continued at the same temperature for 2 hours and at 20° C. for 12 hours. The reaction mixture was poured into ice-water and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was purified by silica gel column chromatography to give 2-[3-(4-phenoxyphenoxy)propyl]pyridine (1.6 g) as pale yellow oil. nD24.5 1.5861.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04970222
Source datasetuspto-grants-1990_11
ORD IDord-4cc41a62c8d2452f9ea35f321c0f698c
Source noteuspto-grants-1990_11