HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006313Generated: October 28, 2026
4-Hydroxybenzaldehyde → 4-Hydroxybenzoic Acid
https://huagongshe.com/reaction/1006313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Product | HCID 13148437 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06787671B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-5db398a221174f439752ee9ed61c13ba |
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| Source note | uspto-grants-2004_09 |
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