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HRID 1082075Erstellt: 26. Oktober 2026

O-Xylene → 4,8-Bis(trifluoromethyl)-10,11-dihydrodibenzo[b,f][1,4]thiazepin-11-one

https://huagongshe.com/reaction/1082075

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktO-XyleneHCID 7237—
EduktSodium HydroxideHCID 14798—
Edukt2-(2-Amino-4-trifluoromethylphenylthio)-3-trifluoromethylbenzonitrileHCID 19969436—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelSulfuric AcidHCID 1118—
Produkt4,8-Bis(trifluoromethyl)-10,11-dihydrodibenzo[b,f][1,4]thiazepin-11-oneHCID 19969457—

Reaktionsschritte

2-(2-Amino-4-trifluoromethylphenylthio)-3-trifluoromethylbenzonitrile (5.43 g, 15 mmol) was dissolved in a mixture of glacial acetic acid (60 ml), concentrated sulphuric acid (55 ml) and water (60 ml) and then heated under reflex for 8 hours. The cooled mixture was added to ice water (500 ml) and brought to pH 4 by addition of 10N aqueous sodium hydroxide. Extraction with dichloromethane followed by filtration, drying (sodium sulphate) and evaporation of the organic layer afforded a residue which was put into xylene (500 ml) and refluxed for 72 hours with azeotropic removal of water. The resulting solution was evaporated and the residue was recrystallised twice from ethanol to give the product as colourless needles (4.30 g, m/s, M+ =363).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05589474
Quelldatensatzuspto-grants-1996_12
ORD IDord-63e5b92100d649e4abe24fe83234f05b
Quellennotizuspto-grants-1996_12