HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 323874Erstellt: 24. Oktober 2026
Potassium Carbonate → 7-Benzyl-1-(4-chlorophenoxymethyl)-3-methylxanthine
https://huagongshe.com/de/reaction/323874
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | alpha,4-Dichloroanisole | HCID 88801 | — |
| Edukt | 7-Benzyl-3-methylxanthine | HCID 685630 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 7-Benzyl-1-(4-chlorophenoxymethyl)-3-methylxanthine | HCID 22007319 | — |
Reaktionsschritte
2.59 g (19.0 mmol) of potassium carbonate were added at 60° C. to a suspension of 3.0 g (12.0 mmol) of 7-benzyl-3-methylxanthine (prepared according to Example 1a) in 50 ml of dimethylformamide and the mixture was stirred at this temperature for one hour. 2.69 g (15.0 mmol) of 4-chlorophenoxymethyl chloride were then added dropwise and the mixture was stirred at 80° C. for 8 hours. The crude mixture was then filtered, the filtrate was concentrated under reduced pressure, the residue was taken up in dichloromethane, and the solution was washed once with 1 N sodium hydroxide solution and twice with water. The organic phases were dried using magnesium sulfate and concentrated under reduced pressure. The crude product was purified by flash chromatography on a silica gel column, dichloromethane/methanol (19.8/0.2) Yield: 4.15 g (87% of theory); melting point: 96° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06214992B1 |
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| Quelldatensatz | uspto-grants-2001_04 |
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| ORD ID | ord-1e17ee0626d943439926e7915051c237 |
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| Quellennotiz | uspto-grants-2001_04 |
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