HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871047Generated: October 30, 2026
Ethyl bromoacetate → HCID 86688755, compound
https://huagongshe.com/reaction/871047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178444930 | HCID 178444930 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 86688755 | HCID 86688755 | — |
Reaction Steps
To a solution of 1-[5-bromo-2-(2-ethyl-butoxy)-benzyl]-1H-pyrazol-3-ol, 3, 0.06 g (0.15 mmol) in acetone (3 mL) was added ethylbromoacetate (24 μL 0.22 mmol), K2CO3 (0.03 g, 0.22 mmol) and tetrabutylammonium iodide (0.008 g, 0.022 mmol). The resulting mixture was heated at 120° C. in an Emrys microwave reactor for 20 min. The volatiles were removed in vacuo and the crude product was purified on silica to yield to {1-[5-Bromo-2-(2-ethyl-butoxy)-benzyl]-1H-pyrazol-3-yloxy}-acetic acid ethyl ester, 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969589B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-20c59bb02b674bdba1748b6686eb8cf8 |
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| Source note | uspto-grants-2015_03 |
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