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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1404639Erstellt: 25. Oktober 2026

4-Hydroxybenzaldehyde → 4-[2-Hydroxy-2-(3-methoxyphenyl)ethoxy]benzaldehyde

https://huagongshe.com/reaction/1404639

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-HydroxybenzaldehydeHCID 126—
EduktSodium HydroxideHCID 14798—
Edukt2-(3-Methoxyphenyl)oxiraneHCID 97903—
LösungsmittelTolueneHCID 1140—
Produkt4-[2-Hydroxy-2-(3-methoxyphenyl)ethoxy]benzaldehydeHCID 81133631122%

Reaktionsbedingungen

Temperatur78 °C

Reaktionsschritte

To a stirring solution of 2-(3-methoxyphenyl)oxirane (5.60 g, 37.0 mmol) in toluene (65 mL) was added 4-hydroxybenzaldehyde (6.80 g, 5.60 mmol), 1M NaOH (65 mL) and PEG4000 (polyethylene glycol, 0.85 g) and the stirring mixture was heated at 78° C. overnight. The reaction mixture was allowed to cool to RT and extracted with EtOAc (2×150 mL). The combined extracts were washed with brine, dried (Na2SO4), filtered and evaporated in vacuo. The resulting light brown oil was chromatographed, eluting with 30-40% EtOAc/hexanes. Fractions containing the higher Rf spot were combined and evaporated in vacuo to give 1.86 g (18%) of the title compound as a clear colorless oil. Fractions containing the lower Rf spot were combined and evaporated in vacuo to give 0.90 g (9%) the regioisomer as a nearly colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08912335B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-61ed0e48f6a740f8beacb012fccf0273
Quellennotizuspto-grants-2014_12