HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606460Generated: October 31, 2026
Ethyl bromoacetate → Ethyl (3-cyanophenoxy)acetate
https://huagongshe.com/reaction/606460
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Cyanophenol | HCID 13394 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl (3-cyanophenoxy)acetate | HCID 24696095 | 101.6% |
Reaction Steps
Ethyl bromoacetate (14.7 g, 88.1 mmol) was added dropwise to a suspension of potassium carbonate (12.8 g, 92.3 mmol) and 3-hydroxybenzonitrile (10.0 g, 83.9 mmol) in THF (50 mL) at room temperature, and the mixture was stirred at 50° C. for 24 hr. The mixture was extracted with ethyl acetate and saturated aqueous ammonium chloride solution, and the organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated to give the title compound as a pale-yellow powder (17.5 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915267B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-41c53868d8584131b7fa8886f4ef2b4c |
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| Source note | uspto-grants-2011_03 |
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