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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 722938생성일: 2026년 10월 25일

5-Chlorovaleryl chloride → 5-Chloro-1-[3-(trifluoroacetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1-pentanone

https://huagongshe.com/reaction/722938

반응식

참여 물질

역할이름HCID투입량
반응물5-Chlorovaleryl chlorideHCID 74089—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물1-(4,5-dihydro-1H-benzo[d]azepin-3(2H)-yl)-2,2,2-trifluoroethanoneHCID 21887139—
용매1,2-DichloroethaneHCID 11—
생성물5-Chloro-1-[3-(trifluoroacetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1-pentanoneHCID 21887301—

반응 단계

Aluminum chloride (17 g, 130 mmol) was added by portions to a solution of 3-(trifluoroacetyl)-2,3,4,5-tetrahydro-1H-3-benzazepine (15.0 g) and 5-chlorovaleryl chloride (8.8 ml) in 1,2-dichloroethane (40 ml) under ice-cooling. After stirring at room temperature for 30 minutes, the reaction mixture was poured into ice (500 g), extracted with ethyl acetate, and washed with brine. The organic layer was dried over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure, and the residue was crystallized from ethanol-diethyl ether to give a pale yellow solid (15.2 g). Further recrystallization from ethanol-diethylether afforded colorless crystals (13.2 g) as the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07138533B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-049ee60c4c134ce78c3c804f230f260d
출처 메모uspto-grants-2006_11