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HRID 1030768作成日:2026年10月27日

Methanol → Digoxin dialdehyde

https://huagongshe.com/reaction/1030768

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物PeriodateHCID 167232—
反応物DigoxinHCID 2724385—
反応物Sodium periodateHCID 23667635—
溶媒Chloroform methanolHCID 21584188—
生成物Digoxin dialdehydeHCID 101931782—

反応手順

Digoxin (0.4985 g, 0.64 mmole) was dissolved in 10 ml of chloroform/methanol (3/1.5) and placed into a 100 ml two-necked flask. Sodium periodate (0.3102 g, 1.4 mmoles) was dissolved in 4 ml distilled water and placed into a pressure equalized addition funnel. The periodate solution was slowly added to the flask while stirring and under nitrogen. A white precipitate was immediately formed and the reaction was complete within 15 minutes after addition of the periodate. Reaction progress was monitored by TLC (E. M. Merck, pre-coated TLC sheets, silica gel 60 F254 0.2 mm thickness) in chloroform/methanol 10/1 by volume Rf 0.16=dialdehyde, one homogeneous spot; Rf 0.07=Digoxin. Both spots became dark brownish when the TLC plate was sprayed with methanol/concentrated sulfuric acid (9/1 by volume) and placed in an oven at 100° C. The reaction mixture was evaporated on a rotatory evaporator and brought up in 30 ml of chloroform and 3 ml of water. The cloudy solution was extracted and the aqueous layer washed three times with 10 ml chloroform. The organic phases are combined (60 ml) and dried over magnesium sulfate. The organic solvents are evaporated to dryness. A light yellow brownish oily material was left. This material was used immediately in the next reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05106963
出典データセットuspto-grants-1992_04
ORD IDord-c5ddd92d08ab40ec9652da27f183b056
出典メモuspto-grants-1992_04