HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711486Generated: October 31, 2026
Hydrogen Peroxide → Methyl 2,4-dichloro-6-hydroxybenzoate
https://huagongshe.com/reaction/1711486
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | 2,4-Dichloro-6-hydroxybenzaldehyde | HCID 528390 | — |
| Catalyst | HCID 178419084 | HCID 178419084 | — |
| Product | Methyl 2,4-dichloro-6-hydroxybenzoate | HCID 21075879 | — |
Reaction Steps
A solution of 2,4-dichloro-6-hydroxybenzaldehyde (5.00 g, 26.18 mmol) in 125 mL methanol was cooled to 0° C. Perchloric acid (70%, 1.47 mL, 16.23 mmol) was added, and the solution was stirred for 10 minutes. To a separate flask, vanadium (V) oxide (0.190 g, 1.05 mmol) was added to a hydrogen peroxide solution (30% in H2O, 11.90 mL, 104.7 mmol) at 0° C. This solution was stirred until the catalyst was dissolved, resulting in a clear orange solution, which was added dropwise to the methanol solution. The reaction was allowed to slowly warm to room temperature and stir overnight. The solution was concentrated under vacuum, and the residue dissolved in ethyl acetate. The organic extract was washed with aqueous sodium bicarbonate and brine, dried over Na2SO4, filtered and concentrated. The residue was filtered through a silica gel plug with 10% ethyl acetate in hexanes to provide methyl 2,4-dichloro-6-hydroxybenzoate that gave proton NMR spectra consistent with theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790754B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-9df57ae126ad481fbcd4cca1f572c36a |
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| Source note | uspto-grants-2010_09 |
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