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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1736451생성일: 2026년 10월 26일

Benzo(B)Thiophene → alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-(benzo[b]thiophene-2-yl)-2-benzo[b]thiophenemethanol

https://huagongshe.com/reaction/1736451

반응식

참여 물질

역할이름HCID투입량
반응물Benzo(B)ThiopheneHCID 7221—
반응물1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinecarboxylic acid, methyl esterHCID 10869587—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-(benzo[b]thiophene-2-yl)-2-benzo[b]thiophenemethanolHCID 18930359—

반응 조건

온도-78 °C

반응 단계

Dissolve benzo[b]thiophene (10.0 g, 74.5 mmol) in anhydrous tetrahydrofuran (100 mL), place under an argon atmosphere and cool to -78° C. Add, by dropwise addition, n-butyllithium (32.79 mL, 81.97 mmol) and stir briefly. Add, by dropwise addition, a solution of 1-[2-(4-methoxyphenyl)ethyl]-4-piperidinecarboxylic acid, methyl ester (20.67 g, 74.52 mmol) in anhydrous tetrahydrofuran (200 mL) and stir at -78° C. for 1.5 hours. Quench with saturated ammonium chloride, separate the organic phase and extract the aqueous phase with ethyl ether. Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo. Purify by chromatography (50% ethyl acetate/hexane) and recrystallize (isopropanol) to give the title compound as a white solid; mp 168°-179° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05541200
출처 데이터셋uspto-grants-1996_07
ORD IDord-ace64f65feda47f8841ed936e502e776
출처 메모uspto-grants-1996_07