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HRID 270037作成日:2026年10月25日

Boron trifluoride etherate → 1-Benzyl-4-(2-fluoro-5-methylbenzyl)piperidin-4-ol

https://huagongshe.com/reaction/270037

反応式

関与物質

役割名称HCID仕込み量
反応物Boron trifluoride etherateHCID 8000—
反応物6-Benzyl-1-oxa-6-azaspiro(2,5)octaneHCID 89238—
反応物3-Bromo-4-fluorotolueneHCID 96745—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-Benzyl-4-(2-fluoro-5-methylbenzyl)piperidin-4-olHCID 59833635—

反応条件

温度-70 °C

反応手順

To a solution of 2-bromo-1-fluoro-4-methylbenzene (0.76 g, 4 mmol) in THF (15 ml) at −70° C. under Ar a solution of n-BuLi (1.6 M in hexane, 2.5 ml, 4 mmol) was added dropwise. The reaction mixture was stirrred at −70° C. for 1 h, then BF3.Et2O (0.5 ml, 4 mmol) was added. After stirring for 20 min at −70° C., a solution of 6-benzyl-1-oxa-6-azaspiro[2.5]octane (0.41 g, 2 mmol) in dry THF (5 ml) was added dropwise. The stirring was continued for 2 h at −70° C., then the reaction mixture was quenched with sat. aq. NH4Cl (20 ml). The layers were separated, the aqueous layer extracted with THF. The combined organic layers were dried over Na2SO4. The solvent was removed in vacuo. Diethyl ether (50 ml) was added to the residue, folowed by a 2 M HCl in Et2O (5 ml). The precipitate was collected, washed with Et2O, and dissolved in minimal volume of methanol (ca. 5 ml). Water (50 ml) was added, and pH adjusted to 10 by addition of 2 M aq. NaOH. The mixture was extracted with ethyl acetate (2×25 ml), and the combined organic extracts were dried with Na2SO4. Evaporation of solvent afforded brownish oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449475B2
出典データセットuspto-grants-2008_11
ORD IDord-150d93bae2494a3b807a6ae59d3dc564
出典メモuspto-grants-2008_11