HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248854Generated: November 4, 2026
Diethylcarbamoyl chloride → HCID 19762011, compound
https://huagongshe.com/reaction/248854
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylcarbamoyl chloride | HCID 6916 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | HCID 178527894 | HCID 178527894 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 19762011 | HCID 19762011 | — |
Reaction Steps
To a flask was added 17.17 g of 1,2,4-triazole-3-thiol and 200 ml of dry tetrahydrofuran. The mixture was stirred under nitrogen at room temperature and 43 ml of diethylcarbamoyl chloride was quickly added dropwise. The mixture was cooled to between 0° C. and 5° C. Dimethylaminopyridine, one gram, was added followed by the slow dropwise addition of 47.4 ml of triethyl amine while maintaining the reaction temperature between 0° C. and 5° C. until all the triethyl amine was added. The mixture became thick and was allowed to warm to room temperature, then was refluxed at 70° C. for about 20 minutes. After the mixture was cooled to room temperature, the volatiles were evaporated off to leave an oily residue. Water, 100 ml, was added to the residue which was then extracted twice with 100 ml portions of ethyl acetate. The ethyl acetate layer was dried using magnesium sulfate and concentrated to a pale yellow solid which was dried thoroughly under vacuum to yield 31.03 g of pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05211739 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-e3be5df152854e5bbedda82daea95cf0 |
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| Source note | uspto-grants-1993_05 |
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