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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892854Generated: October 31, 2026

3-Hydroxybenzaldehyde → Benzaldehyde, 3-(4-fluorophenoxy)-

https://huagongshe.com/reaction/892854

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantPotassium CarbonateHCID 11430—
CatalystCopperHCID 23978—
SolventPyridineHCID 1049—
ProductBenzaldehyde, 3-(4-fluorophenoxy)-HCID 308532073%

Reaction Steps

A heterogeneous mixture of 3-hydroxybenzaldehyde (9.16 g, 75 mmol), 4-bromofluorobenzene (27.30 g, 156 mmol), K2CO3 (16.07 g, 116.3 mmol) and copper powder (2.38 g, 37.5 mmol) in pyridine (75 mL) was refluxed for 40 hrs. It was then cooled to room temperature and filtered through Celite. The filtrate was diluted with ethylacetate (500 mL) and washed with water (3×300 mL). The organic was then dried with MgSO4 and concentrated. The resulting residue was chromatographed (silica gel, hexane:ether, 85:15) to afford 11.83 g (73%) of 3-(4-fluorophenoxy)benzaldehyde as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05120752
Source datasetuspto-grants-1992_06
ORD IDord-d691195a23ed47748117a4e2251b82c3
Source noteuspto-grants-1992_06