HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120272Generated: October 25, 2026
Boron tribromide → 4-(1H-Pyrazol-1-yl)phenol
https://huagongshe.com/reaction/2120272
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 1-(4-Methoxyphenyl)-1H-pyrazole | HCID 12238131 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(1H-Pyrazol-1-yl)phenol | HCID 12463131 | 50% |
Reaction Steps
1-(4-Methoxy-phenyl)-1H-pyrazole (400 mg, 2.30 mmol) was dissolved in methylene chloride (8 ml) and the solution was cooled to −78° C. Boron tribromide (1.0 M in methylene chloride, 5.05 ml) was added dropwise to the solution over about five minutes to afford a brown-colored solution. The reaction mixture was allowed to stir for about thirty minutes, the cooling bath was removed, and the mixture was allowed to stir at room temperature for about an additional three hours. The mixture was poured into water, and the resulting mixture was adjusted to about pH 8. The mixture was extracted with methylene chloride (3×25 ml), and the combined organic layers were dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting crude solid was purified by column chromatography (25% ethyl acetate/hexanes) to afford 183 mg (50% yield) of the desired product as an oil. LRMS ([M+H+])=161.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06689888B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-e6ee05e895d84aba9357d4bdee61e6a1 |
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| Source note | uspto-grants-2004_02 |
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