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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Iodine | HCID 807 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 4-chloro-N-methylpiperidine | HCID 79342 | — |
| 반응물 | 9,10-dihydro-10-methyl-4H-benzo[4,5]cyclohepta-[1,2-b]thiophen-4-one | HCID 23341835 | — |
| 촉매 | 1,2-Dibromoethane | HCID 7839 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 9,10-dihydro-10-methyl-4-(1-methyl-4-piperidyl)-4H-benzo[4,5]cyclohepta-[1,2-b]thiophen-4-ol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04223035 |
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| 출처 데이터셋 | uspto-grants-1980_09 |
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| ORD ID | ord-9c631467525d4903ac5f362e53ff25fa |
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| 출처 메모 | uspto-grants-1980_09 |
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