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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5042생성일: 2026년 10월 26일

Formaldehyde → Methyl 11-[2-(4-methylpiperazino)ethylidene]-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate

https://huagongshe.com/reaction/5042

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Trifluoroacetic acidHCID 6422—
반응물1-MethylpiperazineHCID 53167—
반응물Methyl 1-methylene-6,11-dihydrodibenz[b,e]oxepin-2-carboxylateHCID 19797490—
용매1,1,1,2-TetrachloroethaneHCID 12418—
생성물Methyl 11-[2-(4-methylpiperazino)ethylidene]-6,11-dihydrodibenz[b,e]oxepin-2-carboxylateHCID 53817464—

반응 조건

온도60 °C

반응 단계

1-Methylpiperazine, 30 ml, and 74 g of paraformaldehyde were dissolved in 2 l of tetrachloroethane and 100 ml of trifluoroacetic acid was dropwise added to the solution. After stirring at 60° C. for 2 hours, a solution of 36 g of methyl 1-methylene-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate in 600 ml of tetrachloroethane was dropwise added to the reaction mixture followed by stirring at 90° C. for further 3 hours. The reaction mixture was concentrated to dryness under reduced pressure and 4 N hydrochloric acid aqueous solution was added to the residue to adjust pH to 1. Then, the mixture was washed with diethyl ether. Thereafter, 10 N sodium hydroxide aqueous solution was added to adjust pH to 13. Extraction was performed with 3 l of methylene chloride. After washing with saturated sodium chloride aqueous solution and drying over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was subjected to silica gel column chromatography (eluting solvent; hexane: ethyl acetate: triethylamine=5:5:1) to give 44 g of colorles oily methyl 11-[2-(4-methyl-1-piperazinyl)ethylidene]-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05242931
출처 데이터셋uspto-grants-1993_09
ORD IDord-092a67ae3ade42ac8570afefa1b804a7
출처 메모uspto-grants-1993_09