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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzo(B)Thiophene | HCID 7221 | — |
| 반응물 | 1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinecarboxylic acid, methyl ester | HCID 10869587 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-(benzo[b]thiophene-2-yl)-2-benzo[b]thiophenemethanol | HCID 18930359 | — |
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
| 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-ace64f65feda47f8841ed936e502e776 |
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| 출처 메모 | uspto-grants-1996_07 |
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