HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624005Generated: October 29, 2026
Phenethyl bromide → HCID 58710082, compound
https://huagongshe.com/reaction/624005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-nitro-1H-pyrazole | HCID 16376 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58710082 | HCID 58710082 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09303023B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-5f56696150e8430295920546005f76cd |
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| Source note | uspto-grants-2016_04 |
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