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HRID 1463846作成日:2026年10月25日

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

https://huagongshe.com/reaction/1463846

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HCID 10106958HCID 10106958—
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

4-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 11-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 (eluent; hexane:ethyl acetate:triethylamine=5:5:1) to give 44 g of methyl 11-[2-(4-methyl-1-piperazinyl)ethylidene]-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate as colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05302602
出典データセットuspto-grants-1994_04
ORD IDord-daf8e49dc57d4611a1e4cce99829c589
出典メモuspto-grants-1994_04