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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 562930Erstellt: 25. Oktober 2026

4-Hydroxybenzaldehyde → HCID 60884381, Verbindung

https://huagongshe.com/reaction/562930

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-HydroxybenzaldehydeHCID 126—
EduktSodium HydroxideHCID 14798—
Edukt2-(4-Fluorophenyl)oxiraneHCID 4065230—
LösungsmittelTolueneHCID 1140—
ProduktHCID 60884381HCID 6088438114,1%

Reaktionsbedingungen

Temperatur78 °C

Reaktionsschritte

To 2-(4-fluorophenyl)oxirane (6.50 g, 54.0 mmol) was added toluene (85 ml), 4-hydroxybenzaldehyde (9.89 g, 81.0 mmol), PEG4000 (polyethylene glycol, 1.15 g) and 1M NaOH (85 ml) and the stirring mixture was heated at 78° C. overnight. After cooling to RT the reaction mixture was extracted with EtOAc, and the organic phase was washed with brine, dried (Na2SO4), filtered and evaporated in vacuo. The resulting yellow oil was chromatographed on a medium silica gel column eluting with 0-10% EtOAc/DCM. Fractions containing predominantly the higher Rf spot were combined and evaporated in vacuo to give 1.85 g (14%) of the title compound as a yellow oil. Fractions containing predominantly the lower Rf spot were combined and evaporated in vacuo to give 0.64 g of the regioisomer as a colorless, viscous oil. Mixed fractions were combined and rechromatographed eluting with 30% EtOAc/hexanes. Fractions containing the higher Rf material were combined and evaporated in vacuo to give an additional 2.64 g (20%) of the title compound as a colorless oil. Fractions containing the lower Rf material were combined and evaporated in vacuo to give an additional 1.82 g of the regioisomer as a colorless viscous oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08067450B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-a095e2121563486dabe01d46a5c2e3d9
Quellennotizuspto-grants-2011_11