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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242437Generated: October 26, 2026

2,3,4-Trimethoxy-6-methylbenzaldehyde → 2,3,4-Trimethoxy-6-methylbenzoic acid

https://huagongshe.com/reaction/242437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4-Trimethoxy-6-methylbenzaldehydeHCID 89683—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
SolventDimethyl SulfoxideHCID 679—
Product2,3,4-Trimethoxy-6-methylbenzoic acidHCID 13531415458.1%

Reaction Steps

45.6 g (217 mmol) of 2,3,4-trimethoxy-6-methylbenzaldehyde was dissolved in 130 ml of dimethyl sulfoxide, and an aqueous solution (50 ml) of 5.2 g (44 mmol) of sodium dihydrogen phosphate was dropwise added over a period of 20 minutes. Then, an aqueous solution (180 ml) of 28 g (305 mmol) of sodium chlorite was dropwise added over a period of 3 hours, followed by stirring for 2 hours. A saturated sodium hydrogencarbonate aqueous solution was added until no bubbling occurred, followed by stirring for 1 hour. Then, the reaction solution was washed with 50 ml of ethyl acetate twice, and concentrated hydrochloric acid was added to make the aqueous layer acidic, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate and subjected to filtration, and the solvent was distilled off under reduced pressure. The obtained crystals were washed with hexane to obtain 45.6 g (yield: 93%) of 2,3,4-trimethoxy-6-methylbenzoic acid (melting point 95 to 97° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653113B2
Source datasetuspto-grants-2014_02
ORD IDord-eb5e1b9832af4e1c898d0a2a428ee04d
Source noteuspto-grants-2014_02