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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2211745생성일: 2026년 10월 25일

Hexane → (1-Benzyl-4-piperidyl)(4-isopropylphenyl)(3,4,6-trimethyl-2-methoxyphenyl)methanol

https://huagongshe.com/reaction/2211745

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물2-Bromo-3,5,6-trimethylanisoleHCID 21961310—
반응물1-Benzyl-4-(4-isopropylbenzoyl)piperidineHCID 21961355—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(1-Benzyl-4-piperidyl)(4-isopropylphenyl)(3,4,6-trimethyl-2-methoxyphenyl)methanolHCID 2196135879.2%

반응 단계

To a solution of 2-methoxy-3,4,6-trimethylbromobenzene (15.48 g, 67.56 mmol) in tetrahydrofuran (200 ml), which was kept at −78° C., was added dropwise under an argon atmosphere a solution of n-butyllithium in hexane (1.59 mol/l, 42 ml, 66.78 mmol) and the mixture was stirred for 30 minutes. To this mixture was added dropwise a solution of 1-benzyl-4-(4-isopropylbenzoyl)piperidine (19.81 g, 61.63 mmol) in tetrahydrofuran (50 ml) and the resulting mixture was stirred at room temperature for 30 minutes. Water was added to the reaction mixture and the product was extracted with ethyl acetate. The extracts were washed with an aqueous saturated solution of sodium chloride, dried on magnesium sulfate, filtered, and then concentrated under reduced pressure. The residue was crystallized from ethyl acetate-hexane to obtain 23.01 g (79% yield) of the title compound. Melting point: 154-156° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07101867B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-7a0d3804032f4375ac72b49972c02bc8
출처 메모uspto-grants-2006_09