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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594221Generated: November 2, 2026

(2-Chloro-5-(pyridin-2-yl)phenyl)methanol → 2-Chloro-5-(pyridin-2-yl)benzaldehyde

https://huagongshe.com/reaction/594221

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Chloro-5-(pyridin-2-yl)phenyl)methanolHCID 69083854—
CatalystManganese dioxideHCID 14801—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-5-(pyridin-2-yl)benzaldehydeHCID 86695609—

Reaction Steps

A solution of (2-chloro-5-(pyridin-2-yl)phenyl)methanol (129 mg; 0.72 mmol) in anh. THF (7 ml) was treated with MnO2 (975 mg; 11.22 mmol), and the resulting mixture was stirred at rt, under nitrogen, for 6.5 h. The resulting reaction mixture was then filtered over celite, and the separated solids were washed with THF. The filtrate was concentrated to dryness under reduced pressure giving 2-chloro-5-(pyridin-2-yl)benzaldehyde as a yellow oil. LC-MS (conditions A): tR=0.43 min.; no ionisation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-e499c14df9794d05a477fcdfd2438064
Source noteuspto-grants-2016_01