HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772323Generated: November 3, 2026
Acetic Acid → (4-Bromo-3-methylisoxazol-5-yl)methyl acetate
https://huagongshe.com/reaction/1772323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 12458458 | HCID 12458458 | — |
| Product | (4-Bromo-3-methylisoxazol-5-yl)methyl acetate | HCID 67814794 | 88% |
Reaction Steps
To a solution of (3-methylisoxazol-5-yl)methyl acetate (0.979 g, 6.31 mmol) in AcOH (10 mL, 175 mmol) was added N-bromosuccinimide (1.30 g, 7.30 mmol) and H2SO4 (0.65 mL, 12.19 mmol). The reaction was heated to 110° C. After 1 h, the reaction mixture was cooled to room temperature and carefully poured into a beaker containing ice and saturated NaHCO3. The bi-phasic was vigorously stirred and basic solution (pH˜8-9) was extracted with EtOAc (2×15 mL). The organic layer was washed with 2% sodium thiosulfate, washed with brine (20 mL), dried over Na2SO4, and concentrated to give a light yellow oil. The oil was purified on Biotage system (isocratic elution 10% EtOAc:90% Hexanes) to give the titled compound (1.30 g, 5.55 mmol, 88% Yield) as a colorless yellow oil. LC/MS: m/z 234 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249161B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-b4de2aa1eab2446ab688e8d74876bd8f |
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| Source note | uspto-grants-2016_02 |
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