HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731668Generated: October 30, 2026
Bromine → 2-Bromo-1-(5-cyclopropyl-3-phenyl-isoxazol-4-yl)-ethanone
https://huagongshe.com/reaction/731668
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(5-Cyclopropyl-3-phenyl-isoxazol-4-yl)-ethanone | HCID 67421136 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Bromo-1-(5-cyclopropyl-3-phenyl-isoxazol-4-yl)-ethanone | HCID 24739807 | 96% |
Reaction Steps
To a solution of 1-(5-cyclopropyl-3-phenyl-isoxazol-4-yl)-ethanone (3.34 g, 14.6 mmol) in carbontetrachloride (9.7 mL) and AcOH (0.4 mL) at 48° C. was added a solution of bromine (0.79 mL, 14.6 mmol) in carbontetrachloride (7.8 mL) over 10 min keeping the temperature below 50° C. After addition the reaction mixture was allowed to cool down to room temperature and poured into ice-water (50 mL). The layers were separated and the aqueous layer extracted with dichloromethane. The combined organic layers were then washed with water and brine, dried over sodium sulphate and evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate: 100:0 to 80:20) afforded the title compound (4.29 g, 95%) which was obtained as an off-white solid. MS m/e (EI): 305.0/307.0 [M].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07585874B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-b2e60627a8294d0a8461175471cc4634 |
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| Source note | uspto-grants-2009_09 |
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