Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075539Generated: October 29, 2026

Hydrogen Peroxide → HCID 66701185, compound

https://huagongshe.com/reaction/2075539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodiumHCID 5360545—
ReactantHCID 10632006HCID 10632006—
ReactantSodium ChloriteHCID 23668197—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 66701185HCID 6670118593.7%

Reaction Steps

9.3 g of 4-fluoro-1-methoxynaphthalene-2-carbaldehyde were dissolved in 100 mL of acetonitrile. 2.1 g sodium dihydrogenphsophate monohydrate in 10 mL of water were added, followed by the addition of 9.5 mL hydrogen peroxide (30%). 8.9 g sodium chlorite, dissolved in 20 mL water were added dropwise while maintaining an internal temperature between 5° C. and 15° C. The reaction was then allowed to come to room temp over 2.5 h. The precipitated solid was filtered with suction, and the solid was washed with water, and dried in vacuo at 40° C. to yield 9.4 g of 4-fluoro-1-methoxynaphthalene-2-carboxylic acid. The filtrate was treated with 60 mL of cold 10% aqueous sodium bisulfite solution. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water and brine. The organic layer was washed with 0.2 N NaOH twice. The washes were acidified with 6 N HCl to pH 3, whereupon crystallization occurred. The precipitating product was filtered, washed with water and dried in vacuo at 40° C. to yield a second batch of 1.0 g of 4-fluoro-1-methoxynaphthalene-2-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919628B2
Source datasetuspto-grants-2011_04
ORD IDord-f2e7667457874975858dc41ad511dcec
Source noteuspto-grants-2011_04