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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1-(2-Bromoethyl)-4-methoxybenzene | HCID 84427 | — |
| 반응물 | (Benzo[b]thiophene-3-yl)(4-piperidinyl)methanone | HCID 15337457 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | [Benzo[b]thiophene-3-yl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]methanone | HCID 9799982 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05541200 |
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| 출처 데이터셋 | uspto-grants-1996_07 |
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| ORD ID | ord-d32c1cb8f02c490683939e8dda47f6dc |
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| 출처 메모 | uspto-grants-1996_07 |
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