戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 45158作成日:2026年10月24日

Methyl iodide → (5-Cyclopropyl-4-methyl-isoxazol-3-yl)-carbamic acid phenyl ester

https://huagongshe.com/ja/reaction/45158

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物n-Butyl lithiumHCID 61028—
反応物Acetone cardiceHCID 18522661—
反応物(5-Cyclopropyl-isoxazol-3-yl)-carbamic acid phenyl esterHCID 59394551—
溶媒TetrahydrofuranHCID 8028—
生成物(5-Cyclopropyl-4-methyl-isoxazol-3-yl)-carbamic acid phenyl esterHCID 59394495—

反応条件

温度-78 °C

反応手順

(5-Cyclopropyl-isoxazol-3-yl)-carbamic acid phenyl ester (0.368 g, 1.51 mmol) is dissolved in THF (10 mL) and cooled to −78° C. and flushed with nitrogen. N-butyllithium (2.17 mL, 3.47 mmol) is then added. The mixture is stirred in the dry ice/acetone bath for 30 minutes. Methyl iodide (0.10 mL, 1.66 mmol) is added neat and the reaction is stirred for 2 hours at −78° C. The reaction is quenched (0° C.) with 20 mL of a saturated solution of ammonium chloride, diluted with ethyl acetate and the organic layer is removed, dried (sodium sulfate) and concentrated to an oil that is purified via FCC (0-40% ethyl acetate:heptanes) to give the title compound as an oil. MS (ESI) m/z 259.20 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541432B2
出典データセットuspto-grants-2013_09
ORD IDord-7f3f3842e56e4a07967d61e5674b95f7
出典メモuspto-grants-2013_09