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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270037생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/270037

반응식

참여 물질

역할이름HCID투입량
반응물Boron trifluoride etherateHCID 8000—
반응물6-Benzyl-1-oxa-6-azaspiro(2,5)octaneHCID 89238—
반응물3-Bromo-4-fluorotolueneHCID 96745—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-4-(2-fluoro-5-methylbenzyl)piperidin-4-olHCID 59833635—

반응 조건

온도-70 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449475B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-150d93bae2494a3b807a6ae59d3dc564
출처 메모uspto-grants-2008_11