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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059863Generated: October 25, 2026

Ammonium Chloride → 1-(4-Methoxypyridin-2-yl)propan-2-one

https://huagongshe.com/reaction/1059863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDimethylacetamideHCID 31374—
Reactant4-Methoxy-2-methylpyridineHCID 4737758—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-(4-Methoxypyridin-2-yl)propan-2-oneHCID 18631001—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 2-methyl-4-methoxypyridine (2.03 g) in tetrahydrofuran (20 ml) was added a solution of n-butyllithium in n-hexane (1.63M, 12.1 ml) dropwise at −50° C. under a nitrogen atmosphere, and the mixture was warmed to 0° C. The mixture was cooled to −50° C., and N,N-dimethylacetamide (1.99 ml) was added dropwise. Then the mixture was warmed to room temperature, poured into a saturated aqueous ammonium chloride solution and extracted with ethyl acetate (100 ml×2). The combined organic layer was washed with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography (silica gel 100 g, n-hexane:ethyl acetate=1:2) to give 1-(4-methoxypyridin-2-yl)propan-2-one (2.35 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521643B1
Source datasetuspto-grants-2003_02
ORD IDord-0c8a7b8361f841a183aec70d59e1bb57
Source noteuspto-grants-2003_02