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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 914804생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/914804

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Benzene, 1-(chloromethyl)-2-fluoro-HCID 9580—
반응물Ammonium ChlorideHCID 25517—
반응물1-Benzylpiperidine-4-carbaldehydeHCID 89584—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
용매Ethyl AcetateHCID 8857—
생성물1-(1-Benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanolHCID 2224817362%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07265108B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-2f1eb9591f3944218bac0bfbdd3eb106
출처 메모uspto-grants-2007_09