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HRID 892494作成日:2026年10月26日

Carbon Dioxide → Methyl 11-methoxy-6,11-dihydrodibenz[b,e]oxepin-3-carboxylate

https://huagongshe.com/reaction/892494

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物Sulfuric AcidHCID 1118—
反応物3-Bromo-11-methoxy-6,11-dihydrodibenz[b,e]oxepineHCID 15093136—
反応物HCID 178418244HCID 178418244—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 11-methoxy-6,11-dihydrodibenz[b,e]oxepin-3-carboxylateHCID 9994021—

反応条件

温度-78 °C

反応手順

3-Bromo-11-methoxy-6,11-dihydrodibenz[b,e]oxepine, 30 g, was dissolved in 500 ml of tetrahydrofuran. After cooling to -78° C., 65 ml of 1.6 N n-butyl lithium/hexane solution was dropwise added to the solution in a nitrogen atmosphere followed by stirring at -78° C. for further 40 minutes. The reaction solution was dropwise added onto 100 g of dry ice, which was allowed to stand to elevate to room temperature. The solvent was distilled off under reduced pressure. To the residue obtained, were added 500 ml of methanol and 10 ml of conc. sulfuric acid. The mixture was heated to reflux for 2 hours. After allowing to cool, the solvent was distilled off under reduced pressure. The residue was extracted with 500 ml of ethyl acetate. After washing successively with saturated sodium chloride aqueous solution, saturated sodium bicarbonate aqueous solution and saturated sodium chloride aqueous solution, the extract was dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (eluting solvent; hexane:ethyl acetate=1:1) to give 19.3 g of the product as pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05118701
出典データセットuspto-grants-1992_06
ORD IDord-1e9bdf312ad84b28ad7ca998db7f6bc9
出典メモuspto-grants-1992_06