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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059864Generated: November 3, 2026

Ammonium Chloride → 1-(3-Methoxypyridin-2-yl)propan-2-one

https://huagongshe.com/reaction/1059864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDimethylacetamideHCID 31374—
Reactant3-Methoxy-2-methylpyridineHCID 3015270—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-(3-Methoxypyridin-2-yl)propan-2-oneHCID 18630995—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 3-methoxy-2-methylpyridine (844 mg) in tetrahydrofuran (10 ml) was added a solution of n-butyllithium in n-hexane (1.59M, 5.6 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 (0.955 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). The organic layer was washed with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography (silica gel 50 g, 25% ethyl acetate in n-hexane) to give 1-(3-methoxypyridin-2-yl)propan-2-one (1.12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521643B1
Source datasetuspto-grants-2003_02
ORD IDord-36a5a277a56449e896dd6c43c1344804
Source noteuspto-grants-2003_02