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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2181924생성일: 2026년 10월 27일

Cyclohexene → 3-[(3-Chloro-6-methylphenanthridin-5(6H)-yl)sulfonyl]phenol

https://huagongshe.com/reaction/2181924

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexeneHCID 8079—
반응물Boron tribromideHCID 25134—
반응물3-Chloro-5-[(3-methoxyphenyl)sulfonyl]-6-methyl-5,6-dihydrophenanthridineHCID 22482385—
용매DichloromethaneHCID 6344—
생성물3-[(3-Chloro-6-methylphenanthridin-5(6H)-yl)sulfonyl]phenolHCID 22482291—

반응 단계

A stirred suspension of 3-chloro-5-[(3-methoxyphenyl)sulfonyl]-6-methyl-5,6-dihydrophenanthridine (0.38 g, 0.95 mmol) and cyclohexene (1.73 mL, 17.1 mmol) was treated dropwise at room temperature under nitrogen with a solution of 1.0 M boron tribromide (5.7 mL, 5.7 mmol) in dichloromethane. After stirring for 20 hours at room temperature, the reaction was quenched with a saturated, aqueous sodium bicarbonate solution (50 mL), and extracted with dichloromethane (6×20 mL). The combined organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to a crude residue. The crude residue was triturated with hexane and purified by flash column chromatography, eluting with a mixture of ethyl acetate-hexane (30:70), to afford the title compound as a homogeneous, white, crystalline solid (0.17 g, 73%), m.p. 215° C.;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06894061B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-cc29b6c262b44f47b45a3bc5c2ed9a19
출처 메모uspto-grants-2005_05