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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974813Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
ReactantSodium HydroxideHCID 14798—
Reactant2-(2-Amino-4-trifluoromethylphenylthio)-3-trifluoromethylbenzonitrileHCID 19969436—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product4,8-Bis(trifluoromethyl)-10,11-dihydrodibenzo[b,f][1,4]thiazepin-11-oneHCID 19969457—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607929
Source datasetuspto-grants-1997_03
ORD IDord-17e84a3c41ea44e3a4633a93a698b915
Source noteuspto-grants-1997_03