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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395067Generated: October 30, 2026

(3-(Benzyloxy)pyridin-2-yl)methanol → 3-(Benzyloxy)pyridine-2-carbaldehyde

https://huagongshe.com/reaction/2395067

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-(Benzyloxy)pyridin-2-yl)methanolHCID 13217540—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product3-(Benzyloxy)pyridine-2-carbaldehydeHCID 1337459462%

Reaction Steps

A solution of 3-benzyloxy-2-hydroxymethylpyridine (0.25 g, 1.16 mmol) in chloroform (15 ml) was treated with manganese dioxide (0.45 g, 6.34 mmol). The reaction mixture was heated to reflux and held at reflux for 18 hours. The reaction mixture was then filtered through Celite and evaporated to give a yellow gum. This gum was purified by chromatography (EtOAc/CH2Cl2) to give 3-benzyloxy-2-pyridinecarbaldehyde as a colourless gum (0.15 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811459
Source datasetuspto-grants-1998_09
ORD IDord-0c10ff7049394a2d97d7fba512976412
Source noteuspto-grants-1998_09