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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454518Generated: October 29, 2026

Pyrazole → HCID 58508677, compound

https://huagongshe.com/reaction/454518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantD-ProlineHCID 8988—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-bromo-2-nitrobenzoateHCID 26369829—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 58508677HCID 5850867741.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

1H-Pyrazole (0.14 g), potassium carbonate (0.46 g), D-proline (38 mg), and copper(I) iodide (32 mg) were added to a dimethyl sulfoxide (5 mL) solution of tert-butyl 4-bromo-2-nitrobenzoate (0.50 g), followed by stirring under a nitrogen atmosphere at 100° C. for 3 hours. After cooling the reaction mixture to room temperature, ethyl acetate and water were added thereto, and the insoluble substance was removed by filtration. The organic layer was separated, washed with water and a saturated aqueous solution of sodium chloride sequentially, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [Fuji Silysia Chemical Ltd., PSQ100B (spherical), eluent: 100-80% hexane/ethyl acetate] to obtain 0.20 g of tert-butyl 2-nitro-4-(1H-pyrazol-1-yl)benzoate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-51adc1a33f634014a5efd964de06bad5
Source noteuspto-grants-2013_07