Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894674Generated: November 2, 2026

(4-(Pyridin-2-yloxymethyl)-phenyl)-methanol → 4-((Pyridin-2-yloxy)methyl)benzaldehyde

https://huagongshe.com/reaction/1894674

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-(Pyridin-2-yloxymethyl)-phenyl)-methanolHCID 59255473—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product4-((Pyridin-2-yloxy)methyl)benzaldehydeHCID 5925511842%

Reaction Steps

To a mixture of (4-(pyridin-2-yloxymethyl)-phenyl)-methanol (1.9 g, 8.6 mmol) described in Manufacturing Example 1-1-1 and methylene chloride (30 mL) was added manganese dioxide (15 g, 17 mmol) at room temperature, which was stirred overnight at this temperature. The reaction mixture was filtered through a Celite pad, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:4), to obtain the title compound (770 mg, 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513287B2
Source datasetuspto-grants-2013_08
ORD IDord-06f6b4a98e8c493ea5b6bad431858d02
Source noteuspto-grants-2013_08