HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 563129Erstellt: 25. Oktober 2026
Potassium Iodide → 4-(3-Cyanopropoxy)-7H-furo[3,2-g][1]benzopyran-7-on
https://huagongshe.com/reaction/563129
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-Chlorobutyronitrile | HCID 12336 | — |
| Edukt | Bergaptol | HCID 5280371 | — |
| Lösungsmittel | Methyl Ethyl Ketone | HCID 6569 | — |
| Produkt | 4-(3-Cyanopropoxy)-7H-furo[3,2-g][1]benzopyran-7-on | HCID 11701730 | — |
Reaktionsschritte
800 mg (3.956 mmol) of 5-hydroxypsoralen and 0.7 ml (655.5 mg, 6.33 mmol) of 4-chlorobutyronitrile were refluxed in 50 ml of 2-butanone in the presence of an excess (2.6 g) of anhydrous potassium carbonate and catalytic amounts of potassium iodide for 48 hours. The progress of the reaction was monitored by thin layer chromatography. After 48 hours the reaction mixture was concentrated under reduced pressure. The residual oily layer was cooled, diluted with water and acidified with concentrated hydrochloric acid to pH 1. The slurry was stirred for 15-20 min and then filtered. The solids were washed with water to neutral pH, dried by suction and then further washed with petroleum ether. The dried solids were dissolved in refluxing methanol, treated with charcoal and recrystallized from methanol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08067460B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-ad5f75fd9f024f99a3f39c3987ede021 |
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| Quellennotiz | uspto-grants-2011_11 |
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