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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1743187생성일: 2026년 10월 27일

Water → (4-Isopropylphenyl)-2,2-dimethyl-2,3-dihydrobenzofuran-5-ol

https://huagongshe.com/reaction/1743187

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzene, 2-bromo-1,4-dimethoxy-HCID 91353—
반응물2-(4-Isobutyrylphenyl)propaneHCID 4251244—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(4-Isopropylphenyl)-2,2-dimethyl-2,3-dihydrobenzofuran-5-olHCID 2223826370%

반응 단계

n-Butyllithium (1.6 M, 20.8 mL, 33.2 mmol) was added to a solution of 1-bromo-2,5-dimethoxybenzene (7.2 g, 33.2 mmol) in tetrahydrofuran (20 mL) at −78° C., and the mixture was stirred for 20 minutes at the same temperature. To the reaction mixture was added 1-(4-isopropylphenyl)-2-methylpropan-1-one (5.70 g, 30.0 mmol), and the mixture was stirred for 30 minutes at room temperature. Water (30 mL) was poured into the reaction mixture, which was then extracted three times with ethyl acetate. The organic layers were combined, washed with water, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. A mixture of the residue and 48% hydrobromic acid (30 mL) was heated under reflux for 24 hours in an argon atmosphere. After cooling, water (30 mL) was added to the reaction mixture, which was then extracted twice with ethyl acetate. The organic layers were combined, washed with water, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was crystallized from isopropyl ether-hexane to obtain the title compound (2.1 g, yield 70%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07008950B1
출처 데이터셋uspto-grants-2006_03
ORD IDord-bf47bb5b6d2240ef8c3bbc18a2523bd7
출처 메모uspto-grants-2006_03