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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257519Generated: November 2, 2026

Sodium Carbonate → 2-Chloro-4-pyridinecarboxaldehyde

https://huagongshe.com/reaction/2257519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
ReactantN-bromobutanimideHCID 67184—
Reactant(2-Chloropyridin-4-yl)methanolHCID 7062237—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-4-pyridinecarboxaldehydeHCID 2762994—

Reaction Steps

A suspension of 2-chloro-4-pyridinemethanol (8.0 g, 55.9 mmol), NBS (14.9 g, 83.9 mmol), and K2CO3 (11.75 g, 97.1 mmol) in EtOAc was refluxed for 3 h. A Second portion of NBS (14.9 g, 83.9 mmol) and Na2CO3 (12.0 g, 114 mmol) were added and the reaction was heated to reflux for an additional 3.5 h, cooled and filtered through a pad of celite. The filtrate, after concentrattion to a small volume, was subjected to flash chromatography eluting with 0.5-4% CH3OH/CH2Cl2. The fractions containing product were combined, washed successively with sat aq NaHCO3 10% Na2S2O3, and brine, dried (MgSO4) and concentrated in vacuo to give the title compound as a light yellow solid; yield 5.3 g (67%). 1H NMR (CDCl3) δ 10.06 (s, 1H), 8.66 (d, 1H, J=5.0 Hz), 7.76 (s, 1H), 7.66 (d, 1H, J=5.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658903
Source datasetuspto-grants-1997_08
ORD IDord-cc073a64655d4147b5ca2f83776cf6d9
Source noteuspto-grants-1997_08