HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589099Generated: October 30, 2026
N-bromobutanimide → HCID 67814058, compound
https://huagongshe.com/reaction/589099
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 67814333 | HCID 67814333 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 67814058 | HCID 67814058 | 79% |
Reaction Steps
A solution of (3-methylisoxazol-5-yl)methyl benzoate (20.1 g, 92.4 mmol) in acetic acid (77.3 mL) was treated with N-bromosuccinimide (19.7 g, 111 mmol) and heated in a sealed tube at 90° C. for 4 h. The reaction mixture was diluted with brine and extracted with ethyl acetate. The organic layer was separated, washed with brine, dried over magnesium sulfate, filtered, and concentrated to give the crude product. Purification by flash column chromatography (100% hexanes to 20% ethyl acetate/hexanes) gave the desired product (21.6 g, 79%). LCMS calculated for C12H11BrNO3 (M+H)+: m/z=296.0, 298.0. found: 296.0, 298.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227985B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-b669b41331534a05928d8d454468e18b |
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| Source note | uspto-grants-2016_01 |
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