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HRID 242561作成日:2026年10月25日

Methyl iodide → 1-Benzyl-3,3-dimethylpiperidin-4-one

https://huagongshe.com/reaction/242561

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1-Benzyl-3-methyl-4-piperidoneHCID 560965—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物1-Benzyl-3,3-dimethylpiperidin-4-oneHCID 9794413—

反応手順

To a solution of 1-Benzyl-3-methyl-piperidin-4-one (2.03 g, 10 mmol) in THF (10 mL) was added potassium t-Butoxide (1.1 g, 10 mmol) and methyl iodide (0.62 mL, 10 mmol). The solution was then stirred at room temperature for about 72 hours. The reaction was quenched with brine and extracted with ethyl acetate. The combined organic layers were concentrated in vacuo, then purified by flash chromatography on silica gel (35 g SiO2, gradient elution from 100% hexane to 100% ethyl acetate) to yield the title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653096B2
出典データセットuspto-grants-2014_02
ORD IDord-e58125c1f7014c45afddba3c0a1ec696
出典メモuspto-grants-2014_02