Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 435629생성일: 2026년 10월 25일
Potassium Iodide → 3-[2-[4-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl]-2-oxazolidinone
https://huagongshe.com/reaction/435629
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 3-(2-Chloroethyl)-1,3-oxazolidin-2-one | HCID 75633 | — |
| 반응물 | 1-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-piperazine | HCID 21481142 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 3-[2-[4-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl]-2-oxazolidinone | HCID 21481155 | — |
반응 단계
12.5 g of 1-(2-bromo- 10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-piperazine are treated, together with 13 g of powdered potassium carbonate, 0.2 g of potassium iodide and 1 litre of toluene, with 13.2 g of N-(β-chloroethyl)-oxazolidinone and the mixture is heated under reflux for 25 hours. Then the mixture is poured on to ice-water and diluted with benzene. The benzene solution is washed neutral with water and extracted with 2-N hydrochloric acid. The aqueous phase is made alkaline with sodium hydroxide and extracted with benzene. The organic phase is washed with water, dried over magnesium sulphate and concentrated under reduced pressure. There is obtained crude 3-[2-[4-(2-bromo- 10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl]-2-oxazolidinone which is converted into the maleate of melting point 170°-172° C by treatment with maleic acid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04006145 |
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| 출처 데이터셋 | uspto-grants-1977_02 |
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| ORD ID | ord-3a4ea878bf074d3a9ec01c3364363e42 |
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| 출처 메모 | uspto-grants-1977_02 |
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