HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1814922Erstellt: 25. Oktober 2026
Sodium hydride → 3-(2-Furylmethyl)-7-methylxanthine
https://huagongshe.com/reaction/1814922
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 7-Methylxanthine | HCID 68374 | — |
| Edukt | 2-(Bromomethyl)furan | HCID 4603765 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | 3-(2-Furylmethyl)-7-methylxanthine | HCID 22499127 | 14,3% |
Reaktionsschritte
To a stirring suspension of 7-methylxanthine (2.54 g, 15.3 mmol) in dimethylsulfoxide (80 ml) was added sodium hydride (0.37 mg, 15.3 mmol) in one portion. After stirring for 30 minutes, freshly prepared furfuryl bromide (2.5 g, 15.3 mmol) was added next. After stirring at room temperature for 18 hours, the reaction was quenched by addition of water (150 ml). Saturated aqueous sodium chloride solution (30 ml) was added and the mixture was extracted with chloroform (4×50 ml). The combined extracts were washed with saturated aqueous sodium bicarbonate solution (3×50 ml), with saturated aqueous sodium chloride solution (2×50 ml) and dried over a mixture of sodium sulfate and activated charcoal. After filtration through a pad of celite, the solvent was evaporated under reduced pressure. The residue was treated with ethyl acetate. The solid was filtered, rinsed with cold ethyl acetate (2×25 ml) and vacuum dried to give 3-(2-furylmethyl)-7-methylxanthine (0.54 g, 1496 yield) as a beige solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06878715B1 |
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| Quelldatensatz | uspto-grants-2005_04 |
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| ORD ID | ord-87f5704bb71647279bbd3ed5caaa27f8 |
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| Quellennotiz | uspto-grants-2005_04 |
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