Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006313Generated: October 28, 2026

4-Hydroxybenzaldehyde → 4-Hydroxybenzoic Acid

https://huagongshe.com/reaction/1006313

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
Reactant4-Hydroxybenzoic AcidHCID 135—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventDimethylformamideHCID 6228—
Product4-Hydroxybenzoic AcidHCID 135—
ProductHCID 13148437HCID 13148437—

Reaction Steps

To prepare 4-hydroxy benzoic acid, 4-hydroxybenzaldehyde (100 mg) was dissolved in DMF (10 mL), and OXONE (0.503 g) was added and stirred at room temperature for 18 hours with the reaction having a final volume (11 mL). The reaction was monitored by TLC or GC analysis. EtOAc was added to extract the products and 1N HCl was used to dissolve the salts. The organic extract was washed with 1N HCl (30 mL×3) and brine (30 mL), dried over Na2SO4, and the solvent was removed under reduced pressure to obtain 4-hydroxy benzoic acid in 19% yield and 4-hydroxyphenol formate in 62% yield after purification by silica gel column chromatography. 4-Hydroxyphenyl Formate: 1H NMR (CDCl3, 300 MHz): δ8.27 (s, 1H), 6.98(d, 2H, J=9.0), 6.78 (d, 2H,J=8.9), 5.35 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787671B2
Source datasetuspto-grants-2004_09
ORD IDord-5db398a221174f439752ee9ed61c13ba
Source noteuspto-grants-2004_09