HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895390Generated: November 1, 2026
Ethyl bromoacetate → Ethyl 2-(4-ethylphenoxy)acetate
https://huagongshe.com/reaction/895390
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Ethylphenol | HCID 31242 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 2-(4-ethylphenoxy)acetate | HCID 4501432 | 95.5% |
Reaction Steps
A mixture of 4-ethylphenol (Aldrich) (14.34 g, 116.20 mmoles), anhydrous potassium carbonate (Aldrich) (20.47 g, 146.63 mmoles), ethyl bromoacetate (Aldrich) (17.01 g, 99.81 mmoles) and dry acetone (Aldrich) (200 mL) was refluxed with stirring under a drying tube for 18 hours. The reaction was cooled, and the volatiles were removed by spin evaporation in vacuo. The white residue was partitioned between ice-cold water (250 mL) and dichloromethane (250 mL). The dichloromethane phase was separated and washed with ice cold water (2×100 mL), an ice-cold solution of 5% aqueous sodium hydroxide (150 mL) and finally with ice-cold water (2×100 mL). The dichloromethane solution was dried over sodium sulfate and spin evaporated in vacuo to give 19.86 g (95% yield) of ethyl 4-ethylphenoxyacetate as a clear liquid, which was one spot on thin layer chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06916820B1 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-553b7f7035fe499dbb8cc4dfccba0f68 |
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| Source note | uspto-grants-2005_07 |
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