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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt4-Phenylbenzyl chlorideHCID 15463—
Edukt3-(2-Hydroxyethyl)-7-methoxybenzofuranHCID 22662935—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(2-(4-Phenylbenzyloxy)ethyl)-7-methoxybenzofuranHCID 1835159088,1%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06323235B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-c18d807010494733bd99f084bdb4fdc7
Quellennotizuspto-grants-2001_11