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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31681Generated: October 25, 2026

Acetyl chloride → 4-Chloro-2-methyl-1-oxo-1lambda~5~-pyridine

https://huagongshe.com/reaction/31681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantPyridine, 2-methyl-4-nitro-, 1-oxideHCID 95291—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
Product4-Chloro-2-methyl-1-oxo-1lambda~5~-pyridineHCID 1221180116.8%

Reaction Conditions

Temperature-12.5 °C

Reaction Steps

4-nitro-2-picoline N-oxide (20 g, 130 mmol) was added to acetyl chloride (120 ml, 1688 mmol) in a nitrogen atmosphere at −25° C. The mixture was stirred at −30 to 5° C. for 4 hours and 15 minutes. After the reaction mixture was diluted with ethyl acetate (about 150 ml) and chloroform (about 100 ml), the mixture was concentrated. The residue was purified by silica gel column chromatography (NH silica gel: 200 g, elution solvent: heptane, heptane/ethyl acetate=75/25, 50/50, 25/75, ethyl acetate, ethyl acetate/methanol=20/1) to obtain the title compound (3.14 g) as brown oil. Simultaneously, a crude product (about 17 g) was obtained. The crude product thus obtained was further purified by silica gel column chromatography (NH silica gel: 300 g, elution solvent: heptane, heptane/ethyl acetate=75/25, 40/60, 25/75, ethyl acetate) to obtain the title compound (5.39 g) separately as brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425634B2
Source datasetuspto-grants-2008_09
ORD IDord-b6af840770b1403392ee2ad5c1194c43
Source noteuspto-grants-2008_09