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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762857Generated: October 30, 2026

Pyrazole → 1-(N-(2-isopropylvinyl)-N-tert.-butylcarbamyl)-pyrazole

https://huagongshe.com/reaction/1762857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(2-isopropylvinyl)-N-tert.-butylcarbamyl chlorideHCID 56617464—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product1-(N-(2-isopropylvinyl)-N-tert.-butylcarbamyl)-pyrazoleHCID 5662054564.4%

Reaction Conditions

Temperature40 °C

Reaction Steps

27.2 g (0.2 mole) of pyrazole, 1 g of 4-dimethylaminopyridine and 40.6 g (0.2 mole) of N-(2-isopropylvinyl)-N-tert.-butylcarbamyl chloride are added in succession to a suspension of 42 g of potassium carbonate in 150 ml of dry methylene chloride at 20° C. The mixture is stirred for 10 hours at 40° C., after which the resulting precipitate is filtered off under suction and washed with 200 ml of methylene chloride. The filtrate is washed with three times 80 ml of water, dried over Na2SO4 and evaporated down under reduced pressure, and the oil which remains is evaporated down under reduced pressure. 30.3 g of 1-(N-(2-isopropylvinyl)-N-tert.-butylcarbamyl)-pyrazole are obtained as a colorless liquid of boiling point 104°-105° C./0.3 mbar and nD 1.4828 (Compound No. 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835171
Source datasetuspto-grants-1989_05
ORD IDord-bf9343b70db94b05abd91e64c1dd9577
Source noteuspto-grants-1989_05