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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1947429Erstellt: 26. Oktober 2026

Triethylamine → N-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)methanesulfonamide

https://huagongshe.com/reaction/1947429

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktAmmonium ChlorideHCID 25517—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt2-Iodo-4-nitroanilineHCID 222629—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)methanesulfonamideHCID 6728434480,2%

Reaktionsschritte

To a solution containing 2-iodo-4-nitroaniline (25 g; 95 mmol) and triethylamine (43 ml; 312 mmol) in CH2Cl2 (250 ml), a solution containing methanesulphonyl chloride (36 g; 312 mmol) was added dropwise. The reaction mixture was left under stirring at room temperature for 18 hours, then NH4Cl (saturated solution) was added (250 ml). The biphasic solution was transferred into a separating funnel, the organic phase was separated, dried over Na2SO4 and the solvent was removed by evaporation under reduced pressure. The residue was suspended in EtOH (200 ml) and heated under stirring until a yellow solid precipitated. The crude product was filtered, washed with EtOH (750 ml), and dried under vacuum to give N-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)methanesulfonamide (32 g) which was used in the following reaction without any further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08399477B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-8b96b5f325154a2d842226437a4c4f69
Quellennotizuspto-grants-2013_03