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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1082075생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1082075

반응식

참여 물질

역할이름HCID투입량
반응물O-XyleneHCID 7237—
반응물Sodium HydroxideHCID 14798—
반응물2-(2-Amino-4-trifluoromethylphenylthio)-3-trifluoromethylbenzonitrileHCID 19969436—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매Sulfuric AcidHCID 1118—
생성물4,8-Bis(trifluoromethyl)-10,11-dihydrodibenzo[b,f][1,4]thiazepin-11-oneHCID 19969457—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05589474
출처 데이터셋uspto-grants-1996_12
ORD IDord-63e5b92100d649e4abe24fe83234f05b
출처 메모uspto-grants-1996_12