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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374163Generated: November 3, 2026

Hydrogen Peroxide → Methyl 2,4-dichloro-6-hydroxybenzoate

https://huagongshe.com/reaction/1374163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantMethanolHCID 887—
ReactantPerchloric AcidHCID 24247—
Reactant2,4-Dichloro-6-hydroxybenzaldehydeHCID 528390—
CatalystHCID 178419084HCID 178419084—
ProductMethyl 2,4-dichloro-6-hydroxybenzoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163951B2
Source datasetuspto-grants-2007_01
ORD IDord-1be26c117fb74dde860aba7b33d1750a
Source noteuspto-grants-2007_01