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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1072747Erstellt: 26. Oktober 2026

4-Benzylphenol → 2-(4-Benzyloxyphenyl)-1-[3-(4-benzylphenoxy)propyl]-5-methyl-1H-pyrrole

https://huagongshe.com/reaction/1072747

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BenzylphenolHCID 7563—
EduktTriphenylphosphineHCID 11776—
Edukt1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Edukt3-[2-(4-Benzyloxyphenyl)-5-methyl-1H-pyrrol-1-yl]propan-1-olHCID 22387317—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt2-(4-Benzyloxyphenyl)-1-[3-(4-benzylphenoxy)propyl]-5-methyl-1H-pyrroleHCID 2238758979,6%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of 3-[2-(4-benzyloxyphenyl)-5-methyl-1H-pyrrol-1-yl]propan-1-ol (1.00 g, 3.11 mmol), 4-benzylphenol (572 mg, 3.11 mmol) and triphenylphosphine (1.22 g, 4.67 mmol) in toluene (2 ml) was added 1,1′-(azodicarbonyl)dipiperidine (1.18 g, 4.67 mmol) and the mixture was stirred at 80° C. for 12 hours. The reaction solution was poured into water and the mixture was extracted with ethyl acetate. The extract was dried over magnesium sulfate anhydride and the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=30:1) to give the object compound as an oily substance. 1.21 g (yield: 79.6%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06911468B2
Quelldatensatzuspto-grants-2005_06
ORD IDord-5a525e1ae344464b819331b1ab52c859
Quellennotizuspto-grants-2005_06