Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantIsobutyleneHCID 8255—
Reactant5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylic acidHCID 1519421—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methylpyrazole-3-carboxylateHCID 19356241—

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028084
Source datasetuspto-grants-2000_02
ORD IDord-9129f6b96eff45db94e1d3906d21f3a1
Source noteuspto-grants-2000_02