HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175288Generated: October 29, 2026
Potassium Carbonate → 2-(3-((4-Bromo-1H-pyrazol-1-yl)methyl)phenoxy)ethyl acetate
https://huagongshe.com/reaction/2175288
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Acetoxy-2-bromoethane | HCID 13564 | — |
| Reactant | 3-((4-Bromo-1H-pyrazol-1-yl)methyl)phenol | HCID 70982914 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3-((4-Bromo-1H-pyrazol-1-yl)methyl)phenoxy)ethyl acetate | HCID 70982813 | 34% |
Reaction Steps
A mixture of 3-((4-bromo-1H-pyrazol-1-yl)methyl)phenol (0.6 g, 2.37 mmol), 2-bromoethyl acetate (0.792 g, 4.74 mmol) and potassium carbonate (0.655 g, 4.74 mmol) in DMF (5 mL) was heated at 200° C. in a microwave reactor for 1 h. After this time, the reaction mixture was quenched with water and extracted with ethyl acetate. The organic layer was dried and concentrated. The resulting residue was purified by flash chromatography (0-100% ethyl acetate:hexanes) to afford the title compound (0.27 g, 34% yield) as a colorless oil. LCMS, [M+H]+=339.0. 1H NMR (400 MHz, CDCl3) δ 7.46 (s, 1H), 7.34 (s, 1H), 7.24 (dd, J=8.3, 7.6 Hz, 2H), 6.83 (dd, J=8.3, 2.4 Hz, 1H), 6.80 (d, J=7.6 Hz, 1H), 6.74 (d, J=2.4 Hz, 1H), 5.20 (s, 2H), 4.41-4.32 (m, 2H), 4.14-4.08 (m, 2H), 2.06 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062028B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-ca5dc099bc244b0b8a59fb1957e7d919 |
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| Source note | uspto-grants-2015_06 |
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