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HRID 5042作成日:2026年10月27日

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

https://huagongshe.com/reaction/5042

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Trifluoroacetic acidHCID 6422—
反応物1-MethylpiperazineHCID 53167—
反応物Methyl 1-methylene-6,11-dihydrodibenz[b,e]oxepin-2-carboxylateHCID 19797490—
溶媒1,1,1,2-TetrachloroethaneHCID 12418—
生成物Methyl 11-[2-(4-methylpiperazino)ethylidene]-6,11-dihydrodibenz[b,e]oxepin-2-carboxylateHCID 53817464—

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05242931
出典データセットuspto-grants-1993_09
ORD IDord-092a67ae3ade42ac8570afefa1b804a7
出典メモuspto-grants-1993_09