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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30469Generated: October 25, 2026

(5-Bromo-3-pyridinyl)methanol → 5-Bromo-3-pyridinecarboxaldehyde

https://huagongshe.com/reaction/30469

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Bromo-3-pyridinyl)methanolHCID 2784733—
CatalystManganese dioxideHCID 14801—
Product5-Bromo-3-pyridinecarboxaldehydeHCID 278473451.1%

Reaction Steps

(5-Bromo-pyridin-3-yl)-methanol (1.13 g, 6.00 mmol) was dissolved in CHCI3 (40 mL) and treated with MnO2 (3.60 g). The reaction mixture was heated at reflux temperature for 3 h. The hot reaction mixture was filtered through a pad of diatomaceous earth and the filtrate was concentrated to yield the title compound (0.570 g, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423147B2
Source datasetuspto-grants-2008_09
ORD IDord-a363896c2f4243088d27486a0d5c3e7a
Source noteuspto-grants-2008_09