HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731667Generated: October 26, 2026
5-Cyclopropyl-3-phenyl-isoxazole-4-carboxylic acid methoxy-methyl-amide → 1-(5-Cyclopropyl-3-phenyl-isoxazol-4-yl)-ethanone
https://huagongshe.com/reaction/731667
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Cyclopropyl-3-phenyl-isoxazole-4-carboxylic acid methoxy-methyl-amide | HCID 86613561 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5-Cyclopropyl-3-phenyl-isoxazol-4-yl)-ethanone | HCID 67421136 | 95.8% |
Reaction Steps
To a solution of 5-cyclopropyl-3-phenyl-isoxazole-4-carboxylic acid methoxy-methyl-amide (4.00 g, 14.7 mmol) in THF (42 mL) cooled to −78° C. was added a solution of methylmagnesium bromide (3 M in diethylether, 9.80 mL, 29.4 mmol) dropwise within 5 min at −78° C. The cooling bath was removed and the reaction mixture was allowed to warm up to room temperature over 2.5 h. The reaction mixture was then re-cooled to −78° C., diluted with a saturated ammonium chloride solution (50 mL), allowed to warm up to room temperature and then diluted with water and extracted with ethyl acetate. The combined organic layers were then washed with brine and then dried over sodium sulphate and evaporated to afford the title compound (3.2 g, 94%) which was obtained as a light yellow solid. MS: m/e=228.3 [M+H]+.
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-456dce03e1b4471f85bce7be88940f50 |
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| Source note | uspto-grants-2009_09 |
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