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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41869Generated: October 25, 2026

2-Chloro-3-pyridinecarboxaldehyde → 2-((4-Chlorophenyl)sulfonyl)nicotinaldehyde

https://huagongshe.com/reaction/41869

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-3-pyridinecarboxaldehydeHCID 737607—
ReactantSodium 4-chlorobenzenesulfinateHCID 23664783—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product2-((4-Chlorophenyl)sulfonyl)nicotinaldehydeHCID 5938059246.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Chloro-3-pyridinecarboxaldehyde (5.0 g, 35.0 mmol) and 4-chlorobenzenesulfinic acid sodium salt (7.75 g, 38.8 mmol) were dissolved in DMSO (120 ml) and the mixture was heated at 100° C. for 72 h under nitrogen. Upon cooling to ambient the mixture was diluted with water (500 ml) and extracted with EtOAc (3×). The combined organics were washed with water, brine, dried (MgSO4) and evaporated to dryness to afford 8.1 g of crude material. The crude compound was pre-absorbed onto silica and purified by dry pad suction column chromatography, eluting with heptane using an EtOAc gradient, to afford 4.62 g (61%) of the desired product as a white powdery solid (MP=100.5-101° C.; IR=1698 cm−1; HPLC=8.00 min>99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536158B2
Source datasetuspto-grants-2013_09
ORD IDord-eaf7250bb33344d6979b76e7a6d84fa3
Source noteuspto-grants-2013_09