HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722322Generated: November 1, 2026
Hydrochloric Acid → HCID 178418509, compound
https://huagongshe.com/reaction/1722322
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178418558 | HCID 178418558 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178418509 | HCID 178418509 | 72.1% |
Reaction Steps
After stirring a mixture of 60 g of 2,5-dimercapto-1,3,4-thiadiazole, 25 g of potassium hydroxide, and 750 ml of ethanol for one hour at 70° C., 68 g of ethyl α-bromoacetate was added to the mixture and then the resultant mixture was refluxed for 2 hours. After cooling the reaction mixture, insoluble matters were filtered off and the filtrate thus formed was concentrated under reduced pressure. To the residue thus formed was added 600 ml of 10% sodium hydroxide. The mixture was stirred for one hour at 80° C. After cooling, the reaction mixture was acidified by the addition of concentrated hydrochloric acid (below pH 1) and crystals thus formed were collected by filtration, washed with water, and recrystallized from acetone to provide 60 g of [(5-mercapto-1,3,4-thiadiazol-2-yl)thio]acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04855310 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-59b9b70ceb8045ebbc8d791ed94f0ebf |
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| Source note | uspto-grants-1989_08 |
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