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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368817Generated: November 2, 2026

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

https://huagongshe.com/reaction/1368817

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

At 5° C., 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 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 then stirred for 1 hour at 5° C. and for 12 hours at room temperature. The pH was then adjusted to 1 using 10% strength hydrochloric acid, and 1500 ml of aqueous 40% strength sodium hydrogen sulfite solution were added. After stirring 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. Removal of the solvent by distillation gave 102.0 g of methyl 2-chloro-3-hydroxycarbonyl-4-methylsulfonylbenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576596B1
Source datasetuspto-grants-2003_06
ORD IDord-1eca6bb276074d4f993fbcae728a8d25
Source noteuspto-grants-2003_06