戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1608969作成日:2026年10月25日

Hydroxyamine hydrochloride → Methyl 5-hydroxyimino-4,5-bis(4-methoxyphenyl)-3-pentenoate

https://huagongshe.com/reaction/1608969

反応式

関与物質

役割名称HCID仕込み量
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物Sodium BicarbonateHCID 516892—
反応物Methyl 4,5-bis(4-methoxyphenyl)-5-oxo-3-pentenoateHCID 53769085—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物Methyl 5-hydroxyimino-4,5-bis(4-methoxyphenyl)-3-pentenoateHCID 8530101690%

反応手順

A mixture of 24.5 g of methyl 4,5bis(4-methoxyphenyl)-5-oxo-3-pentenoate and 51.5 g of hydroxylamine hydrochloride in a mixture of 650 ml of methanol and 72 ml of water was heated under reflux for 3 hours. During this procedure, 0.9 equivalent of sodium hydrogen carbonate was added portionwise to the reaction mixture as the reaction progressed. After completion of the reaction, the methanol was distilled off under reduced pressure. Water and ethyl acetate were added to the residue for dissolution thereof, the organic layer was separated, washed with saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The organic layer was then concentrated under reduced pressure and the residue was separated and purified by silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:4) to give 23 g (yield 90%) of methyl 5-hydroxyimino-4,5-bis(4-methoxyphenyl)-3-pentenoate as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05399577
出典データセットuspto-grants-1995_03
ORD IDord-b644e7362b6c44078ff78b1ac12d0222
出典メモuspto-grants-1995_03