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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 637251Erstellt: 26. Oktober 2026

5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chloride → N-[5-(o-chloro-p-trifluoromethyl-phenoxy)-2-nitrobenzoyl]-S,S-dimethyl-sulphoximine

https://huagongshe.com/reaction/637251

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chlorideHCID 3017765—
EduktDimethyl sulphoximine potassium saltHCID 86740516—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
ProduktN-[5-(o-chloro-p-trifluoromethyl-phenoxy)-2-nitrobenzoyl]-S,S-dimethyl-sulphoximineHCID 20256523—

Reaktionsschritte

A solution of 38.01 g of 5-(o-chloro-p-trifluoromethyl-phenoxy)-2-nitrobenzoyl chloride in 125 ml of absolute 1,2-dimethoxyethane is added dropwise at 10°-15° C. while stirring during 30 minutes to a suspension of the dimethyl sulphoximine potassium salt in 250 ml of absolute 1,2-dimethoxyethane. The mixture is stirred at room temperature for 24 hours and subsequently evaporated to dryness under reduced pressure. The resinous residue is dissolved in 1.25 l of diethyl ether, the solution is filtered through Celite and the filtrate is evaporated to dryness. The residue is subsequently purified by chromatography on silica gel with methylene chloride. There is obtained N-[5-(o-chloro-p-trifluoromethyl-phenoxy)-2-nitrobenzoyl]-S,S-dimethyl-sulphoximine as colourless crystals, m.p. 126°-127° C.; 1H-NMR (CDCl3): 7.99 (d,1H), 7.80 (d,1H), 7.60 (q,1H), 7.23 (d,1H) 7.14 (d,1H), 7.02 (q,1H) and 3.40 (s,6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04556413
Quelldatensatzuspto-grants-1985_12
ORD IDord-53afbfdcc1b94f9780874c728e0acec5
Quellennotizuspto-grants-1985_12