HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430783Erstellt: 25. Oktober 2026
Acetic Acid → 3-(2-(4-Phenylbenzyloxy)ethyl)-7-methoxybenzofuran
https://huagongshe.com/reaction/430783
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 4-Phenylbenzyl chloride | HCID 15463 | — |
| Edukt | 3-(2-Hydroxyethyl)-7-methoxybenzofuran | HCID 22662935 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-(2-(4-Phenylbenzyloxy)ethyl)-7-methoxybenzofuran | HCID 18351590 | 88,1% |
Reaktionsschritte
3-(2-hydroxyethyl)-7-methoxybenzofuran (373 mg) was dissolved in DMF (7 ml) and potassium t-butoxide (261 mg) was added to the obtained solution, followed by stirring the resulting solution at room temperature for 20 minutes. To this reaction solution, 4-phenylbenzyl chloride (511 mg) was added and the solution was stirred at room temperature for 1 hour. Acetic acid was added to the reaction solution and the resultant was poured into water layer (50 ml), followed by extraction twice with ethyl acetate (20 ml). The organic layers were combined and washed with saturated brine, followed by drying over sodium sulfate. After removing the sodium sulfate by filtration, the solvent was removed under reduced pressure and the residue was purified by column chromatography (solvent: hexane/ethyl acetate=5/1) using silica gel to obtain the desired compound (613 mg, yield: 88%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06323235B1 |
|---|
| Quelldatensatz | uspto-grants-2001_11 |
|---|
| ORD ID | ord-c18d807010494733bd99f084bdb4fdc7 |
|---|
| Quellennotiz | uspto-grants-2001_11 |
|---|