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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562936Generated: October 27, 2026

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

https://huagongshe.com/reaction/562936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantSodium HydroxideHCID 14798—
Reactant2-(2-Fluorophenyl)oxiraneHCID 14579254—
SolventTolueneHCID 1140—
Product4-[2-(2-Fluorophenyl)-2-hydroxyethoxy]benzaldehydeHCID 8664507211%

Reaction Conditions

Temperature78 °C

Reaction Steps

To a stirring solution of 2-(2-fluorophenyl)oxirane (5.30 g, 38.4 mmol) in toluene (65 ml) was added 4-hydroxybenzaldehyde (7.0 g, 58.0 mmol), 1M NaOH (65 ml) and PEG4000 (polyethylene glycol, 0.85 g) and the stirring mixture was heated at 78° C. overnight. The reaction 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 adsorbed onto silica gel and chromatographed, eluting with 30-40% EtOAc/hexanes. There are 2 major spots. Fractions containing the higher Rf spot were combined and evaporated in vacuo to give 1.10 g (11%) of the title compound as a colorless oil. Fractions containing the lower Rf spot were combined and evaporated in vacuo to give 0.67 g (7%) of the regioisomer as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067450B2
Source datasetuspto-grants-2011_11
ORD IDord-698a41a28cd74233928391278d2dec9d
Source noteuspto-grants-2011_11