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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27696생성일: 2026년 10월 24일

Iodine → 9,10-dihydro-10-methyl-4-(1-methyl-4-piperidyl)-4H-benzo[4,5]cyclohepta-[1,2-b]thiophen-4-ol

https://huagongshe.com/ko/reaction/27696

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Ammonium ChlorideHCID 25517—
반응물4-chloro-N-methylpiperidineHCID 79342—
반응물9,10-dihydro-10-methyl-4H-benzo[4,5]cyclohepta-[1,2-b]thiophen-4-oneHCID 23341835—
촉매1,2-DibromoethaneHCID 7839—
용매TetrahydrofuranHCID 8028—
생성물9,10-dihydro-10-methyl-4-(1-methyl-4-piperidyl)-4H-benzo[4,5]cyclohepta-[1,2-b]thiophen-4-olHCID 23341831—

반응 단계

4.8 g of iodine-activated magnesium are covered with a layer of 60 cc of anhydrous tetrahydrofuran and cauterized with a few drops of ethylene bromide. A solution of 25.0 g of 4-chloro-1-methylpiperidine in 160 cc of anhydrous tetrahydrofuran is then added dropwise at such a rate that the solvent boils continually, and stirring is subsequently effected at the boil for 2 hours. The reaction mixture is cooled to 10°, and a solution of 20.0 g of 9,10-dihydro-10-methyl-4H-benzo[4,5]cyclohepta-[1,2-b]thiophen-4-one in 100 cc of anhydrous tetrahydrofuran is added dropwise at this temperature. After stirring at room temperature for 11/2 hours and at the boil for 30 minutes, the reaction mixture is cooled, poured on 300 cc of a 20% ammonium chloride solution, and the organic phase is separated. The aqueous solution is extracted with methylene chloride, the combined organic solutions are washed with water, dried over sodium sulphate and concentrated by evaporation. The 9,10-dihydro-10-methyl-4-(1-methyl-4-piperidyl)-4H-benzo[4,5]cyclohepta-[1,2-b]thiophen-4-ol, obtained as residue, is recrystallized twice from isopropanol. M.P. 177°-178°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04223035
출처 데이터셋uspto-grants-1980_09
ORD IDord-9c631467525d4903ac5f362e53ff25fa
출처 메모uspto-grants-1980_09