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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638298Generated: November 3, 2026

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

https://huagongshe.com/reaction/1638298

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 thyl 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 numberUS04879292
Source datasetuspto-grants-1989_11
ORD IDord-73949e8ad96649d8877ce53ad9d86397
Source noteuspto-grants-1989_11