Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Periodate | HCID 167232 | — |
| Reactant | Digoxin | HCID 2724385 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | HCID 101931782 | HCID 101931782 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05106963 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-c5ddd92d08ab40ec9652da27f183b056 |
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| Source note | uspto-grants-1992_04 |
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