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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353377Generated: October 26, 2026

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

https://huagongshe.com/reaction/2353377

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-3-pyridinecarboxaldehydeHCID 737607—
Reactant4-fluorobenzenesulfinic acid sodium saltHCID 23666220—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product2-((4-Fluorophenyl)sulfonyl)nicotinaldehydeHCID 59380583545.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Chloro-3-pyridinecarboxaldehyde (4.04 g, 2.86 mmol) and 4-fluorobenzenesulfinic acid sodium salt (5.73 g, 3.14 mmol) were dissolved in DMSO (100 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 7.89 g of crude product. 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 4.14 g (41%) of the desired product as a yellow solid (plates) (MP=131-131.3° C.; IR=1691 cm−1; HPLC=7.21 min>99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750027B2
Source datasetuspto-grants-2010_07
ORD IDord-8c156ed3576f45de8f270204af544227
Source noteuspto-grants-2010_07