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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219406Generated: October 27, 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/2219406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Cyclopropyl-3-phenyl-isoxazole-4-carboxylic acid methoxy-methyl-amideHCID 86613561—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Cyclopropyl-3-phenyl-isoxazol-4-yl)-ethanoneHCID 6742113695.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414061B2
Source datasetuspto-grants-2008_08
ORD IDord-bc45c8c870b04db4935af2b7fe4facf6
Source noteuspto-grants-2008_08