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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyrazole | HCID 1048 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(2-isopropylvinyl)-N-tert.-butylcarbamyl chloride | HCID 56617464 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(N-(2-isopropylvinyl)-N-tert.-butylcarbamyl)-pyrazole | HCID 56620545 | 64.4% |
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
| 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-bf9343b70db94b05abd91e64c1dd9577 |
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| Source note | uspto-grants-1989_05 |
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