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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1736433생성일: 2026년 10월 25일

Trifluoroacetic acid → [Benzo[b]thiophene-3-yl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]methanone

https://huagongshe.com/reaction/1736433

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Potassium CarbonateHCID 11430—
반응물1-(2-Bromoethyl)-4-methoxybenzeneHCID 84427—
반응물(Benzo[b]thiophene-3-yl)(4-piperidinyl)methanoneHCID 15337457—
용매DimethylformamideHCID 6228—
생성물[Benzo[b]thiophene-3-yl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]methanoneHCID 9799982—

반응 조건

온도90 °C

반응 단계

Mix (benzo[b]thiophene-3-yl)(4-piperidinyl)methanone.CF3CO2H (2.0 g, 5.56 mmol), 2-(4-methoxyphenyl)ethyl bromide (1.27 g, 5.93 mmol), potassium carbonate (1.95 g, 1.41 mmol) and anhydrous dimethylformamide (20 mL). Warm to approximately 90° C. and stir overnight. Allow to cool to room temperature and partition between a 2:1 mixture of ethyl acetate:toluene and water. Separate the aqueous phase and wash the organic phase with water and saturated sodium chloride. Dry (Na2SO4) and evaporate the solvent in vacuo. Purify by chromatography (40% ethyl acetate/hexane) and recrystallize (cyclohexane) to give the title compound as pale yellow plates; mp 114°-116° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05541200
출처 데이터셋uspto-grants-1996_07
ORD IDord-d32c1cb8f02c490683939e8dda47f6dc
출처 메모uspto-grants-1996_07