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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199242Generated: November 3, 2026

Hydrochloric Acid → HCID 15114333, compound

https://huagongshe.com/reaction/1199242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
ReactantEthanethiolHCID 6343—
ReactantSodium HydroxideHCID 14798—
Reactant2,3-Dichloro-4-(ethanesulfonyl)benzoic acidHCID 2764249—
Solvent1,2-DichloroethaneHCID 11—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 15114333HCID 15114333—
ProductHCID 178437384HCID 178437384—

Reaction Steps

A solution of the 4-ethylsulfonyl-2,3-dichlorobenzoic acid prepared in Example 3 (0.2 mole), ethyl mercaptan (0.8 mole), sodium hydroxide (1 mole) in water (300 ml) was heated at reflux for 24 hours. After cooling, the reaction mixture was acidified with concentrated hydrochloric acid and extracted with methylene chloride. The layers were separated, and the methylene chloride layer was dried over magnesium sulfate. Evaporation of the methylene chloride in vacuo then afforded a mixture of the acids which were esterified to the methyl esters with methanol and sulfuric acid in ethylene dichloride by the procedure of Clinton and Lawkowski, J. Amer. Chem. Soc., 70, 3135 (1948). The esters were then separated via standard chromatographic techniques. Basic hydrolysis of each methyl ester then afforded the 3,4-bis-ethylthio-2-chlorobenzoic acid, m.p. 73°-75° C. and 2-chloro-4-ethylsulfonyl-3-ethylthio-benzoic acid oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04898973
Source datasetuspto-grants-1990_02
ORD IDord-1fe14d30331a4fe1ad33c58a73205cb5
Source noteuspto-grants-1990_02