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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274332Generated: October 31, 2026

4-Hydroxybenzaldehyde → 4-[2-(3-Fluorophenyl)-2-hydroxyethoxy]benzaldehyde

https://huagongshe.com/reaction/2274332

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantSodium HydroxideHCID 14798—
Reactant2-(3-Fluorophenyl)oxiraneHCID 15293916—
SolventTolueneHCID 1140—
Product4-[2-(3-Fluorophenyl)-2-hydroxyethoxy]benzaldehydeHCID 8664507417%

Reaction Conditions

Temperature78 °C

Reaction Steps

To a stirring solution of 2-(3-fluorophenyl)oxirane (5.60 g, 40.5 mmol) in toluene (65 mL) was added 4-hydroxybenzaldehyde (7.40 g, 61.0 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 then 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 to give 2 major spots. Fractions containing the higher Rf spot were combined and evaporated in vacuo to give 1.78 g (17%) of the title compound as a white solid. Fractions containing the lower Rf spot were combined and evaporated in vacuo to give 0.90 g (9%) of the regioisomer as a nearly colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126959B2
Source datasetuspto-grants-2015_09
ORD IDord-3f2d05e0d00247e294a8bbda1483e6cc
Source noteuspto-grants-2015_09