Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730865Generated: October 30, 2026

(5,6-Dichloropyridin-3-yl)methanol → 5,6-Dichloropyridine-3-carbaldehyde

https://huagongshe.com/reaction/730865

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5,6-Dichloropyridin-3-yl)methanolHCID 21882961—
CatalystManganese dioxideHCID 14801—
SolventMethylenechloride HexaneHCID 21226440—
Product5,6-Dichloropyridine-3-carbaldehydeHCID 11535654—

Reaction Steps

A mixture of (5,6-dichloro-pyridin-3-yl)-methanol (1.78 g, 10 mmol, TCI-US) and MnO2 (17.39 g, 200 mmol, Aldrich) in 1:1 CH2Cl2/hexane (10 ml) was stirred at room temperature for 1 h. The catalyst was filtered and washed with 50% EtOAc/hexane. The filtrate was evaporated and the residue dried in vacuo to give the title compound product, which was used in the next step without additional purification. MS (ESI, pos. ion) m/z: 176 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582761B2
Source datasetuspto-grants-2009_09
ORD IDord-e8e6b4a92cf84553a65abfbc4f4fd6b5
Source noteuspto-grants-2009_09