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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624005Generated: October 29, 2026

Phenethyl bromide → HCID 58710082, compound

https://huagongshe.com/reaction/624005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantCesium carbonateHCID 10796—
Reactant4-nitro-1H-pyrazoleHCID 16376—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 58710082HCID 58710082—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-nitro-1H-pyrazole (1.50 g, 12.87 mmol) in MeCN (30 mL), (2-bromoethyl)benzene (1.97 mL, 14.15 mmol) and Cs2CO3 (4.61 g, 14.15 mmol) was added. The resulting mixture was refluxed (80° C.) for 1.5 h, then the reaction mixture was allowed to reach rt. The mixture was diluted with DCM, filtered, the filter cake was washed with DCM and the filtrate was concentrated in vacuo to obtain 4-nitro-1-phenethyl-1H-pyrazole as a beige solid which was used in the next step without further purification. LC-MS conditions A: tR=0.92 min; [M+H]+=217.97.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303023B2
Source datasetuspto-grants-2016_04
ORD IDord-5f56696150e8430295920546005f76cd
Source noteuspto-grants-2016_04