HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172147Generated: October 31, 2026
Hydrochloric Acid → Methyl 3-[3-(4-trifluoromethoxy-phenyl)-pyrazol-1-yl]-benzoate
https://huagongshe.com/reaction/2172147
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 3-(Methoxycarbonyl)benzeneboronic acid | HCID 2734714 | — |
| Reactant | HCID 178506361 | HCID 178506361 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-[3-(4-trifluoromethoxy-phenyl)-pyrazol-1-yl]-benzoate | HCID 66616070 | — |
Reaction Steps
A solution of 3-(4-trifluoromethoxy-phenyl)-1H-pyrazole (250 mg), 3-methoxycarbonylphenylboronic acid (540 mg) and pyridine (0.18 mL) in dimethylformamide (5 mL) is treated with copper (II) acetate (214 mg) and powdered activated 4 Å molecular sieves (0.5 g). The resulting mixture is heated to 60° C. for 16 h and cooled. The reaction mixture is poured into 1M aq. HCl (300 mL), and the resulting mixture is filtered through a glass microfiber filter pad. The pad is washed with ethyl acetate, and the filtrate is evaporated to afford the product, methyl 3-[3-(4-trifluoromethoxy-phenyl)-pyrazol-1-yl]-benzoate, as a solid (204 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051342B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-7b7ab0aa440d4ed2b8cc46cd18bc1079 |
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| Source note | uspto-grants-2015_06 |
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