HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721925Generated: October 28, 2026
Bromoacetic Acid → [2,3-Dichloro-4-(1-ethoxymethyl-5-pyrazolylcarbonyl)phenoxy]acetic acid
https://huagongshe.com/reaction/1721925
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetic Acid | HCID 6227 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 14622774 | HCID 14622774 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | [2,3-Dichloro-4-(1-ethoxymethyl-5-pyrazolylcarbonyl)phenoxy]acetic acid | HCID 9864296 | 56.3% |
Reaction Steps
0.63 g of 2,3-dichloro-4-(1-ethoxymethyl-5-pyrazolylcarbonyl)phenol, 0.58 g of bromoacetic acid and 1.11 g of potassium carbonate are added to 40 ml of acetone, and the mixture is refluxed for 48 hours. The reaction mixture is concentrated to remove solvent, and water is added to the residue. The aqueous mixture is washed with ethyl acetate, acidified with 10% hydrochloric acid and then extracted with ethyl acetate. The extract is washed with a saturated sodium chloride solution, dried and evaporated to remove solvent. The residue is crystallized with water, and the crystals are separated by filtration, washed successively with water and isopropyl ether, and dried to give 0.42 g of [2,3-dichloro-4-(1-ethoxymethyl-5-pyrazolylcarbonyl)phenoxy]acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853404 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-bae290b93c5c434d85ea6ad0188b6633 |
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| Source note | uspto-grants-1989_08 |
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