HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762856Generated: October 31, 2026
1,2,4-Triazolylsodium → 1-(N-(2-isopropylvinyl)-N-tert.-butylcarbamoyl)-1,2,4-triazole
https://huagongshe.com/reaction/1762856
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2,4-Triazolylsodium | HCID 54719965 | — |
| Reactant | N-(2-isopropylvinyl)-N-tert.-butylcarbamyl chloride | HCID 56617464 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(N-(2-isopropylvinyl)-N-tert.-butylcarbamoyl)-1,2,4-triazole | HCID 56606765 | 55.9% |
Reaction Steps
21 g (0.103 mole) of N-(2-isopropylvinyl)-N-tert.-butylcarbamyl chloride are added dropwise to a suspension of 10.5 g (0.115 mole) of sodium 1,2,4-triazolide in 100 ml of dry tetrahydrofuran at 20° C. The mixture is stirred for 6 hours at 65° C., after which it is cooled to 20° C., the resulting precipitate is filtered off under suction, the filtrate is evaporated down and the oil which remains is distilled under reduced pressure. 13.6 g of 1-(N-(2-isopropylvinyl)-N-tert.-butylcarbamoyl)-1,2,4-triazole are obtained as a colorless liquid of boiling point 95°-97° C./0.15 mbar and nD 1.4815 (Compound No. 2)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04835171 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-b55449881a2146afa5550dec17bf16e3 |
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| Source note | uspto-grants-1989_05 |
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