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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 616884생성일: 2026년 10월 25일

Hydrofluoric Acid → 5-benzyl-10-fluoro-5H-dibenz[b,f]azepine

https://huagongshe.com/reaction/616884

반응식

참여 물질

역할이름HCID투입량
반응물Hydrofluoric AcidHCID 14917—
반응물Sulfur tetrafluorideHCID 24555—
반응물5-Benzyl-10-oxo-10,11-dihydro-5H-dibenz[b,f]azepineHCID 13352932—
용매DichloromethaneHCID 6344—
생성물5-benzyl-10-fluoro-5H-dibenz[b,f]azepineHCID 20366407—

반응 단계

A mixture of 149.7 g (0.5 mole) of 5-benzyl-5,11-dihydro-10H-dibenz[b,f]azepin-10-one (vide British Pat. No. 961 444),27 ml of hydrogen fluoride, 125 g of sulphur tetrafluoride and 400 ml of methylene chloride is heated in a steel autocalve for 16 hours to 70° C. After the mixture has cooled, the bulk of the liquid constituents are filtered off with suction. Then water and aqueous ammonia solution are added until the pH of the aqueous phase is 9-10. The organic phase is separated, washed three times with water, diluted with 200 ml of benzene and concentrated in a rotary evaporator. The black residue is dissolved in methylene chloride and the solution is filtered through 700 g of silica gel (particle size 0.063-0.2 mm) with methylene chloride as eluant. The filtrate is concentrated, the residue dissolved in 1.5 liters of benzene and stirred for 30 minutes with 500 g of magnesium silicate gel. The mixture is filtered and 500 g of magnesium silicate gel are again added to the filtrate. After repeated filtration, the solution is concentrated in vacuo and the black residue is chromatographed over 800 g of silica gel (particle size 0.063-0.2 mm) with hexane/benzene (2:1) as eluant. The homogeneous fractions are combined and concentrated to yield the 5-benzyl-10-fluoro-5H-dibenz[b,f]azepine as a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04076812
출처 데이터셋uspto-grants-1978_02
ORD IDord-6e16e1d325b246158c6043cb965b24b3
출처 메모uspto-grants-1978_02