HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710614Generated: November 2, 2026
Ethyl bromoacetate → (4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetic acid
https://huagongshe.com/reaction/710614
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazole | HCID 1206965 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetic acid | HCID 1876853 | 84.1% |
Reaction Steps
To a solution of 4-chloro-5-methyl-3-(trifluoromethyl)pyrazole (15 g, 81.3 mmol) in DMF (82 mL) was added ethyl 2-bromoacetate (13.6 g, 81.3 mmol) and potassium carbonate (12.4 g, 89.4 mmol). The mixture was heated at 55° C. for 10 hours with stirring. After cooling to room temperature, the reaction mixture was diluted with water (100 mL) and extracted with ethyl acetate (3×150 mL). The combined organic layers were washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (SiO2, 0-30% ethyl acetate in hexanes) to afford the desired product (18.5 g, 68.4 mmol, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181241B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-f4dba391d020462b9fe73839d26908f6 |
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| Source note | uspto-grants-2015_11 |
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