Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1743199생성일: 2026년 10월 27일
Water → (1-Benzyl-4-piperidyl)(2,5-dimethoxy-3,4,6-trimethylphenyl)(4-isopropylphenyl)methanol
https://huagongshe.com/reaction/1743199
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 1-Bromo-2,5-dimethoxy-3,4,6-trimethylbenzene | HCID 297365 | — |
| 반응물 | 1-Benzyl-4-(4-isopropylbenzoyl)piperidine | HCID 21961355 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (1-Benzyl-4-piperidyl)(2,5-dimethoxy-3,4,6-trimethylphenyl)(4-isopropylphenyl)methanol | HCID 22238283 | 83.6% |
반응 단계
n-Butyllithium (1.6 M, 12.0 mL, 19.2 mmol) was added to a solution of 1-bromo-2,5-dimethoxy-3,4,6-trimethylbenzene (4.89 g, 18.87 mmol) in tetrahydrofuran (100 mL) at −78° C., and the mixture was stirred for 30 minutes at the same temperature. To the reaction mixture was added 1-benzyl-4-(4-isopropylbenzoyl)piperidine (5.02 g, 15.6 mmol). The mixture was stirred for 30 minutes at the same temperature, then poured into the water, and extracted twice with ethyl acetate. The organic layers were combined, washed with an aqueous saturated sodium hydrogencarbonate, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was crystallized from ethyl acetate-hexane to obtain the title compound (6.54 g, yield 83%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07008950B1 |
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| 출처 데이터셋 | uspto-grants-2006_03 |
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| ORD ID | ord-90be5dc8b3344adf87a097b2ca3a0bd2 |
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| 출처 메모 | uspto-grants-2006_03 |
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