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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930299Generated: October 30, 2026

(6-Chloro-4-(phenylamino)pyridin-3-yl)methanol → 6-Chloro-4-phenylamino-pyridine-3-carbaldehyde

https://huagongshe.com/reaction/1930299

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Chloro-4-(phenylamino)pyridin-3-yl)methanolHCID 86620159—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product6-Chloro-4-phenylamino-pyridine-3-carbaldehydeHCID 5921234886%

Reaction Steps

MnO2 (39 g, 448 mmol) was added to a solution of (6-chloro-4-phenylamino-pyridin-3-yl)-methanol (13 g, 56 mmol) in CH2Cl2 (100 ml) and the mixture was stirred at RT overnight. The solids was removed by filtration and the filtrate was concentrated to give 6-chloro-4-(phenylamino)nicotinaldehyde (11 g, 86% yield). 1H-NMR (400 MHz, DMSO-d6): δ 10.18 (s, 1H), 9.99 (s, 1 H), 8.62 (s, 1 H), 7.49-7.31 (m, 5 H), 6.80 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188113B2
Source datasetuspto-grants-2012_05
ORD IDord-ebf072c8500f416f8157b4968a82ffd2
Source noteuspto-grants-2012_05