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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557260Generated: October 26, 2026

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

https://huagongshe.com/reaction/557260

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-(Pyridin-2-yloxymethyl)-phenyl)-methanolHCID 59255473—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product4-((Pyridin-2-yloxy)methyl)benzaldehydeHCID 59255118—

Reaction Steps

To a mixture of (4-(pyridin-2-yloxymethyl)-phenyl)methanol described in Preparation Example 1-3-1 (1.9 g, 8.6 mmol) 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 bed, and the solvent thereof 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058444B2
Source datasetuspto-grants-2011_11
ORD IDord-643ba2afb7614979a979497b77b99a84
Source noteuspto-grants-2011_11