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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,4-TriazolylsodiumHCID 54719965—
ReactantN-(2-isopropylvinyl)-N-tert.-butylcarbamyl chlorideHCID 56617464—
SolventTetrahydrofuranHCID 8028—
Product1-(N-(2-isopropylvinyl)-N-tert.-butylcarbamoyl)-1,2,4-triazoleHCID 5660676555.9%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835171
Source datasetuspto-grants-1989_05
ORD IDord-b55449881a2146afa5550dec17bf16e3
Source noteuspto-grants-1989_05