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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248020Generated: November 1, 2026

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

https://huagongshe.com/reaction/2248020

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 numberUS05037853
Source datasetuspto-grants-1991_08
ORD IDord-1209d6fdb25640d4a2c9075b97a2d6fc
Source noteuspto-grants-1991_08