Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059870Generated: November 1, 2026

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

https://huagongshe.com/reaction/1059870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDimethylacetamideHCID 31374—
Reactant4-Isopropyloxy-2-methylpyridineHCID 18667573—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-(4-Isopropyloxypyridin-2-yl)-propan-2-oneHCID 18667608—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-isopropyloxy-2-methylpyridine (687 mg) in tetrahydrofuran (7 ml) was added a solution of n-butyllithium in n-hexane (1.63M, 3.34 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 (0.549 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-(4-isopropyloxypyridin-2-yl)-propan-2-one (652 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521643B1
Source datasetuspto-grants-2003_02
ORD IDord-3011af2c39534fe99e088b6b1340c6ef
Source noteuspto-grants-2003_02