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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1294714Erstellt: 25. Oktober 2026

Pyridine → 2,4-Dinitrobenzenesulfonamide

https://huagongshe.com/reaction/1294714

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktTrifluoroacetic acidHCID 6422—
EduktSulfuryl chlorideHCID 24648—
EduktBenzenesulfonyl chloride, 2,4-dinitro-HCID 74255—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,4-DinitrobenzenesulfonamideHCID 10911854—

Reaktionsschritte

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

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07241780B2
Quelldatensatzuspto-grants-2007_07
ORD IDord-9a6f3c68a27c48d99b239b56849d49a4
Quellennotizuspto-grants-2007_07