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HRID 974813作成日:2026年10月25日

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

https://huagongshe.com/reaction/974813

反応式

関与物質

役割名称HCID仕込み量
反応物O-XyleneHCID 7237—
反応物Sodium HydroxideHCID 14798—
反応物2-(2-Amino-4-trifluoromethylphenylthio)-3-trifluoromethylbenzonitrileHCID 19969436—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒Sulfuric AcidHCID 1118—
生成物4,8-Bis(trifluoromethyl)-10,11-dihydrodibenzo[b,f][1,4]thiazepin-11-oneHCID 19969457—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05607929
出典データセットuspto-grants-1997_03
ORD IDord-17e84a3c41ea44e3a4633a93a698b915
出典メモuspto-grants-1997_03