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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786694Generated: October 26, 2026

1-(6-Chloro-3-methoxy-pyridazin-4-yl)-propan-1-ol → 1-(6-Chloro-3-methoxy-pyridazin-4-yl)-propan-1-one

https://huagongshe.com/reaction/1786694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(6-Chloro-3-methoxy-pyridazin-4-yl)-propan-1-olHCID 10262280—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product1-(6-Chloro-3-methoxy-pyridazin-4-yl)-propan-1-oneHCID 23092489—

Reaction Steps

12.25 g 1-(6-Chloro-3-methoxy-pyridazin-4-yl)-propan-1-ol is dissolved in 410 ml tetrahydrofuran and 105 g of manganese dioxide is added. The reaction is stirred for 24 h at RT. Solids are removed by filtration, and the solution is treated with a further 105 g of manganese dioxide for 16 h at RT. Solids are removed by filtration, and the solvent is removed under reduced pressure. The product is purified by silica gel chromatography, eluting with a gradient of ethyl acetate in heptane. Yield 3.25 g. LC-MS (ES+) 201 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507734B2
Source datasetuspto-grants-2009_03
ORD IDord-695cb214ce6b4accb0e739d2448d5410
Source noteuspto-grants-2009_03