Back
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

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 numberUS07790754B2
Source datasetuspto-grants-2010_09
ORD IDord-9df57ae126ad481fbcd4cca1f572c36a
Source noteuspto-grants-2010_09