Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826864Generated: October 25, 2026

Pyridine → 2,4-Dinitrobenzenesulfonamide

https://huagongshe.com/reaction/1826864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSulfuryl chlorideHCID 24648—
ReactantBenzenesulfonyl chloride, 2,4-dinitro-HCID 74255—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2,4-DinitrobenzenesulfonamideHCID 10911854—

Reaction Steps

A solution of Part A compound (1.01 g, 2.37 mmol) and TFA (8 mL) in CH2Cl2 (30 mL) was stirred at RT for 4.5 h. The solution was concentrated in vacuo, and the residue was dissolved in CH2Cl2 and filtered through a pad of solid K2CO3. The filtrate was concentrated in vacuo to give the corresponding crude amine. To a solution of the crude amine in THF (11.9 mL) were added pyridine (0.383 mL, 4.74 mmol) and 2,4-dinitrobenzenesulfonyl chloride (0.85 g, 3.19 mmol) and the solution was stirred at RT for 15 h. Since some starting material still remained at this point, more sulfonyl chloride (0.32 g, 1.2 mmol) was then added. After a further 4 h, HPLC analysis indicated that all starting material had been consumed. The reaction mixture was diluted with Et2O, washed with 1N aq HCl, saturated aq NaHCO3 and brine, dried (MgSO4), filtered and concentrated in vacuo to provide the crude 2,4-dinitrobenzenesulfonamide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053106B2
Source datasetuspto-grants-2006_05
ORD IDord-a252d30743f84e0c84e4b8fb15cedf05
Source noteuspto-grants-2006_05