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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276119Generated: October 31, 2026

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

https://huagongshe.com/reaction/1276119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium ChlorideHCID 5234—
ReactantPhosphoric acid, disodium salt, hydrateHCID 61488—
ReactantMethyl 2-chloro-3-formyl-4-methylsulfonylbenzoateHCID 18517410—
ReactantSodium BisulfiteHCID 23665763—
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 a 30% strength solution of hydrogen peroxide and 66.2 g (0.59 mol) of an 80% strength aqueous sodium chloride solution were added successively 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 at 5° C. for 1 hour and then at room temperature for 12 hours. 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. The mixture was stirred at room temperature for 1 hour and the aqueous phase was extracted three times with ethyl acetate. The combined organic phases were washed with sodium hydrogen sulfite solution and dried. The solvent was distilled off, yielding 102.0 g of methyl 2-chloro-3-hydroxycarbonyl-4-methylsulfonylbenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06165944
Source datasetuspto-grants-2000_12
ORD IDord-0f2f3b3e043b4135bb196d3103e24d0e
Source noteuspto-grants-2000_12