Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594265Generated: October 25, 2026

(5-Chloro-6-(difluoromethoxy)pyridin-3-yl)methanol → 3-Pyridinecarboxaldehyde, 5-chloro-6-(difluoromethoxy)-

https://huagongshe.com/reaction/594265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Chloro-6-(difluoromethoxy)pyridin-3-yl)methanolHCID 69085757—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product3-Pyridinecarboxaldehyde, 5-chloro-6-(difluoromethoxy)-HCID 86695614—

Reaction Steps

A solution of (5-chloro-6-(difluoromethoxy)pyridin-3-yl)methanol (1.000 g; 4.77 mmol) in anh. DCM (40 ml) was treated with MnO2 (6.222 g; 71.57 mmol), and the resulting mixture was stirred at rt, under nitrogen, for 3 h. The resulting reaction mixture was then filtered over celite, and the separated solids were washed with DCM. The filtrate was concentrated to dryness under reduced pressure giving 5-chloro-6-(difluoromethoxy)nicotinaldehyde as a yellow oil. LC-MS (conditions A): tR=0.72 min.; no ionisation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-736790edd7574fd6b78bae7863fd29ac
Source noteuspto-grants-2016_01