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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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물3-(2-Chloroethyl)-1,3-oxazolidin-2-oneHCID 75633—
반응물1-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-piperazineHCID 21481142—
용매BenzeneHCID 241—
용매TolueneHCID 1140—
생성물3-[2-[4-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl]-2-oxazolidinoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04006145
출처 데이터셋uspto-grants-1977_02
ORD IDord-3a4ea878bf074d3a9ec01c3364363e42
출처 메모uspto-grants-1977_02