HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201990Generated: October 29, 2026
Potassium Carbonate → methyl 3-(1-methyl-1H-pyrazol-5-yl)benzoate
https://huagongshe.com/reaction/2201990
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 3-(Methoxycarbonyl)benzeneboronic acid | HCID 2734714 | — |
| Reactant | 5-Bromo-1-methyl-1H-pyrazole | HCID 17933381 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Product | methyl 3-(1-methyl-1H-pyrazol-5-yl)benzoate | HCID 69687203 | 83.6% |
Reaction Steps
A mixture of (3-(methoxycarbonyl)phenyl)boronic acid (270 mg, 1.5 mmol), 5-bromo-1-methyl-1H-pyrazole (200 mg, 1.25 mmol), K2CO3 (518 mg, 3.75 mmol) and Pd(dppf)Cl2 (10 mg) in a mixture solution of dioxane (8 mL) and H2O (2 mL) was stirred at 120° C. for 30 min under microwave heating. The catalyst was filtered and the filtrate concentrated. The residue was then purified by column chromatography to give provide the desired product as a colorless oil (226 mg, Yield 60%). It was used directly in the next step. LCMS (m/z): 217.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365519B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-3c84ec2475c9491d8310fee9fbcffafa |
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| Source note | uspto-grants-2016_06 |
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