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HRID 606150作成日:2026年10月26日

Iodine → 1-(1-Benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanol

https://huagongshe.com/reaction/606150

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Benzene, 1-(chloromethyl)-2-fluoro-HCID 9580—
反応物Ammonium ChlorideHCID 25517—
反応物1-Benzylpiperidine-4-carbaldehydeHCID 89584—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
溶媒Ethyl AcetateHCID 8857—
生成物1-(1-Benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanolHCID 2224817362%

反応手順

After suspending 1.84 g of magnesium in 20 ml of diethyl ether, a catalytic amount of iodine was added, a portion of a diethyl ether solution (70 ml) containing 9.97 g of 2-fluorobenzyl chloride was added dropwise while stirring, and the mixture was heated to initiate the reaction. The remaining solution was then added dropwise at a rate to maintain reflux. After 10 minutes, the mixture was cooled on ice, a diethyl ether solution (70 ml) containing 15.4 g of 1-benzyl-4-piperidinecarboxaldehyde [CAS No. 22065-85-6] was added dropwise, and stirring was continued for 20 minutes. Saturated aqueous ammonium chloride solution was added to the reaction solution and extraction was performed with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by NH silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain the title compound (13.4 g, 62% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07915274B2
出典データセットuspto-grants-2011_03
ORD IDord-1cb3489aa30b4a7db07404ec3690db4f
出典メモuspto-grants-2011_03