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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547613Generated: October 28, 2026

4-Hydroxybenzaldehyde → HCID 54893623, compound

https://huagongshe.com/reaction/547613

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-nitrotolueneHCID 94956—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 54893623HCID 54893623104.5%

Reaction Steps

4-Hydroxybenzaldehyde (945 mg, 7.7 mmol), 4-fluoro-2-methyl-1-nitrobenzene (1.0 g, 6.4 mmol), and K2CO3 (1.77 g, 12.8 mmol) were stirred in 55 mL dimethylformamide at 100 degrees Centigrade for 18 hours. The reaction was cooled to room temperature, diluted with ethylacetate, extracted two times with 1N NaOH, and rinsed with brine. The organic layer was dried over MgSO4, filtered and concentrated to afford 1.72 g crude 4-[(3-methyl-4-nitrophenyl)oxy]benzaldehyde, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939528B2
Source datasetuspto-grants-2011_05
ORD IDord-60d9335a37a446f692712dd700cf9931
Source noteuspto-grants-2011_05