HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19066Generated: October 27, 2026
Benzoyl Peroxide → 4-Bromo-3-(4-methoxy-phenoxy)-but-2-enoic acid ethyl ester
https://huagongshe.com/reaction/19066
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-(4-Methoxy-phenoxy)-but-2-enoic acid ethyl ester | HCID 66894795 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-Bromo-3-(4-methoxy-phenoxy)-but-2-enoic acid ethyl ester | HCID 66895435 | 78.4% |
Reaction Steps
A solution of 3-(4-methoxy-phenoxy)-but-2-enoic acid ethyl ester (0.98 g, 4.17 mmol) in carbon tetrachloride (23.2 mL) was treated with N-bromosuccinimide (0.81 g, 4.59 mmol) and benzoyl peroxide (81 mg, 0.33 mmol). The reaction was then heated to reflux for 5 h. At this time, the reaction was cooled to 25° C. and then was placed in the freezer over the weekend. At this time, the reaction was removed from the freezer and allowed to thaw. The resulting precipitate was removed by filtration and was rinsed with carbon tetrachloride (5 mL). The filtrate was concentrated in vacuo. Purification by Analogix flash chromatography (40 g, 1-4% ethyl acetate/hexanes) afforded impure 4-bromo-3-(4-methoxy-phenoxy)-but-2-enoic acid ethyl ester (1.03 g, 78%) as a pale, yellow oil. The material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741327B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-007e44bde25340908035797ba6283bda |
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| Source note | uspto-grants-2010_06 |
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