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HRID 974813Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/974813

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 reflux 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
PatentnummerUS05607929
Quelldatensatzuspto-grants-1997_03
ORD IDord-17e84a3c41ea44e3a4633a93a698b915
Quellennotizuspto-grants-1997_03