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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377543Generated: October 30, 2026

Hydrochloric Acid → Methyl 2-chloro-3-hydroxycarbonyl-4-methylsulfonylbenzoate

https://huagongshe.com/reaction/377543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantPhosphoric acid, disodium salt, hydrateHCID 61488—
ReactantMethyl 2-chloro-3-formyl-4-methylsulfonylbenzoateHCID 18517410—
ReactantSodium BisulfiteHCID 23665763—
ReactantSodium ChloriteHCID 23668197—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-chloro-3-hydroxycarbonyl-4-methylsulfonylbenzoateHCID 18517418—

Reaction Conditions

Temperature5 °C

Reaction Steps

13.8 g (0.11 mol) of sodium hydrogen phosphate monohydrate in 170 ml of water, 49.3 g (0.43 mol) of 30% strength hydrogen peroxide solution and 66.2 g (0.59 mol) of 80% strength aqueous sodium chlorite solution were added in succession at 5° C. to a solution of 115.3 g (0.42 mol) of methyl 2-chloro-3-formyl-4-methylsulfonylbenzoate and 2000 ml of acetonitrile. The reaction solution was subsequently stirred for 1 hour at 5° C. and for 12 hours at room temperature. The pH was then brought to 1 using 10% strength hydrochloric acid, and 1500 ml of aqueous 40% strength sodium hydrogen sulfite solution were added. After the mixture had been stirred for 1 hour at room temperature, the aqueous phase was extracted three times with ethyl acetate. The combined organic phases were washed with sodium hydrogen sulfite solution and dried. After the solvent had been distilled off, 102.0 g of methyl 2-chloro-3-hydroxycarbonyl-4-methylsulfonylbenzoate were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028035
Source datasetuspto-grants-2000_02
ORD IDord-d9df11de04c349f3934a0c3b39541094
Source noteuspto-grants-2000_02