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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

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-Bromo-2,5-dimethoxy-3,4,6-trimethylbenzeneHCID 297365—
반응물1-Benzyl-4-(4-isopropylbenzoyl)piperidineHCID 21961355—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(1-Benzyl-4-piperidyl)(2,5-dimethoxy-3,4,6-trimethylphenyl)(4-isopropylphenyl)methanolHCID 2223828383.6%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07008950B1
출처 데이터셋uspto-grants-2006_03
ORD IDord-90be5dc8b3344adf87a097b2ca3a0bd2
출처 메모uspto-grants-2006_03