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HRID 561266作成日:2026年10月27日

Methyl iodide → 1-Benzyl-3,5-dimethylpiperidin-4-one

https://huagongshe.com/reaction/561266

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Lithium HexamethyldisilazideHCID 2733832—
溶媒TetrahydrofuranHCID 8028—
生成物1-Benzyl-3,5-dimethylpiperidin-4-oneHCID 2227892031.5%

反応条件

温度-78 °C

反応手順

To a −78° C. solution of 1-benzyl-3-methyl-piperidin-4-one (4.06 g, 20 mmol) in anhydrous THF (20 mL) was added lithium hexamethyldisilazide (21 mL, 21 mmol of a 1.0 M solution THF). After being stirred at −78° C. for 30 min, a solution of iodomethane (1.31 mL, 21 mmol) in THF (5 mL) was added into the reaction mixture. The resultant solution was stirred at 25° C. for 2 h and quenched with water. The aqueous layer was extracted with CH2Cl2. The organic extracts were combined, washed with brine and dried over MgSO4. The solution was filtered and concentrated in vacuo to give the crude product. The crude material was purified by flash column chromatography (hexane/EtOAc) to provide 1.37 g (31.5% yield) of 1-benzyl-3,5-dimethyl-piperidin-4-one.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063222B2
出典データセットuspto-grants-2011_11
ORD IDord-2d3b74bdf7674fbabcccd1ce21f23f2c
出典メモuspto-grants-2011_11