HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507950Generated: November 2, 2026
Dimethylformamide → {4-[(3-tert-butyl-5-phenyl-1H-pyrazol-1-yl)methyl]phenyl}methanol
https://huagongshe.com/reaction/507950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | [4-(Chloromethyl)phenyl]methanol | HCID 5107660 | — |
| Reactant | HCID 178440651 | HCID 178440651 | — |
| Solvent | Water | HCID 962 | — |
| Product | {4-[(3-tert-butyl-5-phenyl-1H-pyrazol-1-yl)methyl]phenyl}methanol | HCID 23157326 | 20% |
Reaction Steps
A mixture of 3-tert-butyl-5-phenyl-1H-pyrazole (2.0 g, 10 mmol), 4-(chloromethyl)benzyl alcohol (1.70 g, 10.8 mmol), potassium carbonate (2.76 g, 20 mmol) and N,N-dimethylformamide (20 mL) was stirred at 120° C. for 2 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (5%-80% ethyl acetate/hexane) to give the title compound (640 mg, yield 20%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786165B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-544dfbc6bebf45f0b8c56d2f0b874118 |
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| Source note | uspto-grants-2010_08 |
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