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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 401779Erstellt: 24. Oktober 2026

Triethylamine → 3-Chloro-4-({[3-chloro-4-(trifluoromethyl)benzyl]amino}carbonyl)benzenesulfonyl chloride

https://huagongshe.com/de/reaction/401779

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-Chloro-4-(chlorosulfonyl)benzoyl chlorideHCID 19814731—
Edukt3-Chloro-4-(trifluoromethyl)benzylamineHCID 23512744—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-Chloro-4-({[3-chloro-4-(trifluoromethyl)benzyl]amino}carbonyl)benzenesulfonyl chlorideHCID 5773211640,7%

Reaktionsschritte

To a solution of 2-chloro-4-(chlorosulfonyl)benzoyl chloride (J. Org. Chem., 56,16, 1991, 4974) (300 mg, 0.877 mmol, 1 eq) in DCM (3 ml) was added 3-chloro-4-(trifluoromethyl)benzylamine (175 mg, 0.835 mmol, 0.95 eq) and Et3N (33 mg, 0.32 mmol, 0.37 eq) and the reaction mixture stirred at room temperature for 1 hour. The reaction mixture was diluted with ethyl acetate (10 ml), washed with water (10 ml), dried over sodium sulphate, filtered and evaporated. The crude material was purified by column chromatography eluting with ethyl acetate to yield the title compound (154 mg, 0.34 mmol, 39%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08741934B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-d756446f2c68467997e93dcdcb194469
Quellennotizuspto-grants-2014_06