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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1665002Erstellt: 24. Oktober 2026

Diisopropylethylamine → N-(5-bromo-thiophen-2-ylmethyl)-2-trifluoromethyl-benzenesulfonamide

https://huagongshe.com/de/reaction/1665002

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt2-Trifluoromethylbenzenesulphonyl chlorideHCID 136616—
Edukt(5-Bromothiophen-2-yl)methanamineHCID 23130577—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(5-bromo-thiophen-2-ylmethyl)-2-trifluoromethyl-benzenesulfonamideHCID 3540889757,2%

Reaktionsschritte

To a stirred suspension of 1-(5-bromo-2-thienyl)-methanamine (0.5 g) in dichloromethane (8 mL) were added 2-(trifluoromethyl)-benzenesulfonyl chloride (0.67 g) and N-ethyl-diisopropylamine (0.37 g) at 0° C. After stirring for 10 min, the ice bath was removed and the mixture was stirred for 40 min. The reaction mixture was diluted with dichloromethane and washed with 0.5 M HCl and with water. The organic phase was dried (MgSO4), filtered and concentrated. The residue was suspended in cyclohexane. The solid was collected by filtration and dried to give N-(5-bromo-thiophen-2-ylmethyl)-2-trifluoromethyl-benzenesulfonamide (0.596 g) as a colorless solid. MS: 417.1 ([M+NH4]+)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08039493B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-dc894f865cda4f85bea1c75c570400e6
Quellennotizuspto-grants-2011_10