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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462907Generated: October 31, 2026

Hydrochloric Acid → HCID 13336751, compound

https://huagongshe.com/reaction/1462907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantSodium HydroxideHCID 14798—
ReactantSodium ThiosulfateHCID 24477—
ReactantHCID 13336749HCID 13336749—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 13336751HCID 13336751—

Reaction Steps

(±)-1,2,3,4-Tetrahydro-1-(3-mercapto-1-oxopropyl)-2-quinolinecarboxylic acid (13.27 g) was suspended in water (125 ml) and the pH was adjusted to 6-7 by the addition of 2 N sodium hydroxide. To the resulting clear solution was added 0.5 M iodine in 95% ethanol dropwise while maintaining the pH at 6.5 by the slow addition of 2 N sodium hydroxide. When a yellow color remained for at least five minutes, addition of the iodine solution was termined and the color was discharged with saturated aqueous sodium thiosulfate. The mixture was then acidified with concentrated hydrochloric acid and extracted with ethyl acetate. The combined organic layer was washed with 10% hydrochloric acid and water, dried over magnesium sulfate, and concentrated under reduced pressure to yield 11 g of (±) 1,1'-[dithiobis(1-oxo-3,1-propanediyl]-bis-1,2,3,4-tetrahydro-2-quinolinecarboxylic acid, m.p. 92°-103° (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04461896
Source datasetuspto-grants-1984_07
ORD IDord-53de944d66b940739d2b9beec9275c18
Source noteuspto-grants-1984_07