HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377637Generated: October 30, 2026
Sulfuric Acid → Tert-butyl 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methylpyrazole-3-carboxylate
https://huagongshe.com/reaction/377637
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | 5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylic acid | HCID 1519421 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Tert-butyl 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methylpyrazole-3-carboxylate | HCID 19356241 | — |
Reaction Steps
A solution of 5 g of 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methylpyrazole-3-carboxylic acid in 35 ml of dioxane is introduced into a 250 ml autoclave and then cooled to -10° C. 2 ml of concentrated H2SO4 and 70 ml of 2-methylpropene, cooled to -10° C., are then added and the autoclave is closed, allowed to warm up to RT and then heated at 40° C. for 18 hours, with vigorous stirring. After cooling to RT, the reaction mixture is concentrated under vacuum, the residue is extracted with DCM, the organic phase is washed with water, with 5% Na2CO3 solution and with saturated NaCl solution and dried over MgSO4 and the solvent is evaporated off under vacuum. The residue is chromatographed on silica using a toluene/AcOEt mixture (from 90/10 to 80/20; v/v) as the eluent to give 3.15 g of the expected product, m.p.=112° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06028084 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-9129f6b96eff45db94e1d3906d21f3a1 |
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| Source note | uspto-grants-2000_02 |
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