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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Phosphoric acid, disodium salt, hydrate | HCID 61488 | — |
| Reactant | Methyl 2-chloro-3-formyl-4-methylsulfonylbenzoate | HCID 18517410 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-chloro-3-hydroxycarbonyl-4-methylsulfonylbenzoate | HCID 18517418 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06576596B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-1eca6bb276074d4f993fbcae728a8d25 |
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| Source note | uspto-grants-2003_06 |
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