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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | 1-Methylpiperazine | HCID 53167 | — |
| 반응물 | Methyl 1-methylene-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate | HCID 19797490 | — |
| 용매 | 1,1,1,2-Tetrachloroethane | HCID 12418 | — |
| 생성물 | Methyl 11-[2-(4-methylpiperazino)ethylidene]-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate | HCID 53817464 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05242931 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-092a67ae3ade42ac8570afefa1b804a7 |
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| 출처 메모 | uspto-grants-1993_09 |
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