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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786674Generated: October 30, 2026

HCID 10397613, compound → 1-(6-Chloro-3-methoxy-4-pyridazinyl)ethanone

https://huagongshe.com/reaction/1786674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10397613HCID 10397613—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product1-(6-Chloro-3-methoxy-4-pyridazinyl)ethanoneHCID 23092491—

Reaction Steps

3.85 g 1-(6-Chloro-3-methoxy-pyridazin-4-yl)-ethanol is dissolved in 300 ml tetrahydrofuran and 35.5 g of manganese dioxide is added. The reaction is stirred for 48 h at RT. Solids are removed by filtration, and the solvent is removed under reduced pressure. The product is purified and separated from 1-(3-chloro-6-methoxy-pyridazin-4-yl)-ethanone by silica gel chromatography, eluting with a gradient of ethyl acetate in heptane. Yield 2.4 g. LC-MS (ES+) 187 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507734B2
Source datasetuspto-grants-2009_03
ORD IDord-4e0a1926184942ec9626622b11249023
Source noteuspto-grants-2009_03