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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249669Generated: October 29, 2026

Hydrochloric Acid → 3-(Methoxycarbonylmethyl)-4-isobutoxybenzoic acid

https://huagongshe.com/reaction/2249669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantMethyl 2-(5-formyl-2-isobutoxyphenyl)acetateHCID 17816550—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
Product3-(Methoxycarbonylmethyl)-4-isobutoxybenzoic acidHCID 1781652672.8%

Reaction Conditions

Temperature7.5 °C

Reaction Steps

In 8 ml of acetonitrile is dissolved 0.80 g of methyl 2-(5-formyl-2-isobutoxyphenyl)acetate. After successively adding 2.03 g of sodium dihydrogen-phosphate dissolved in 25 ml of water, 0.69 ml of 30% aqueous hydrogen peroxide and 0.73 g of sodium chlorite dissolved in 15 ml of water at a temperature of 5-10° C., the mixture thus obtained is stirred at 5-10° C. for 3.5 hours. Chloroform and water are added to the reaction mixture, pH is adjusted to 2.0 with 6 mol/L hydrochloric acid, and the organic layer is separated. The organic layer thus obtained is washed with water and saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, and then the solvent is distilled off under reduced pressure. Thus, 0.62 g of 3-(methoxycarbonylmethyl)-4-isobutoxybenzoic acid is obtained as a colorless crystalline product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-b6000604f322432fa50978a2d001169a
Source noteuspto-grants-2008_01