HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499106Generated: November 2, 2026
1-Bromo-4-chloro-2-fluorobenzene → HCID 25212417, compound
https://huagongshe.com/reaction/1499106
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-4-chloro-2-fluorobenzene | HCID 137275 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178428694 | HCID 178428694 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 25212417 | HCID 25212417 | — |
| Product | 1-(2-bromo-5-chlorophenyl)-5-methyl-1H-pyrazole | HCID 57609541 | — |
Reaction Steps
Potassium t-butoxide (3.9 g, 0.33 mmol) was dissolved in DMSO (25 mL). To this solution was added 3-methylpyrazole (2.7 g, 0.33 mmol) and the reaction was heated at 50° C. for 30 min. 1-Bromo-4-chloro-2-fluorobenzene (4.6 g, 0.22 mmol) was then added and the reaction was stirred at 50° C. for 16 h. The reaction was cooled to RT and extracted with water and EtOAc, washed with brine, and dried over Na2SO4, filtered and concentrated in vacuo. Purification by normal phase silica gel column chromatography (EtOAc/heptane) provided 1-(2-bromo-5-chlorophenyl)-3-methyl-1H-pyrazole and 1-(2-bromo-5-chlorophenyl)-5-methyl-1H-pyrazole as a 4:1 mixture that was used in the next step directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199994B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-00ee8b2838d8438391b49ff0abd64f8c |
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| Source note | uspto-grants-2015_12 |
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