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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(2-Fluorophenyl)oxirane | HCID 14579254 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[2-(2-Fluorophenyl)-2-hydroxyethoxy]benzaldehyde | HCID 86645072 | 11% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067450B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-698a41a28cd74233928391278d2dec9d |
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| Source note | uspto-grants-2011_11 |
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