HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860095Generated: October 31, 2026
N-bromobutanimide → Ethyl 3-(3-bromo4-hydroxyphenyl)-2-phenoxypropionate
https://huagongshe.com/reaction/1860095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 3-(4-hydroxyphenyl)-2-phenoxypropionate | HCID 18625748 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 3-(3-bromo4-hydroxyphenyl)-2-phenoxypropionate | HCID 18625875 | 77.3% |
Reaction Steps
N-bromosuccinimide (1.12 g) was added to a solution of ethyl 3-(4-hydroxyphenyl)-2-phenoxypropionate (1.43 g), which is the product of reference example 4(c) in chloroform (20 ml) at ambient temperature. The mixture was stirred at 70° C. for 4 hour and concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water. The ethyl acetate layer was separated and washed with saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified via chromatography on silica gel column using hexane/ethyl acetate=4/1 as the eluant to afford the desired compound (1.41 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06528525B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-5bd58bb5f8344a2ab587f222083a1c02 |
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| Source note | uspto-grants-2003_03 |
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