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HRID 852088생성일: 2026년 10월 26일

Diisopropylamine → 2-Chloro-alpha-(3-methoxyphenyl)-3-pyridinemethanol

https://huagongshe.com/reaction/852088

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물2-ChloropyridineHCID 7977—
반응물3-MethoxybenzaldehydeHCID 11569—
반응물Ammonium ChlorideHCID 25517—
반응물Lithium diisopropylamideHCID 2724682—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물2-Chloro-alpha-(3-methoxyphenyl)-3-pyridinemethanolHCID 2014573351%

반응 단계

Combine 2.5 M n-butyl lithium in hexane (40 mL), diisopropyl amine (14 mL, 0.10 mol) and cold (−68° C.) tetrahydrofuran (250 mL) and stir for 20 minutes, to generate lithium diisopropylamide. Add 2-chloro-pyridine (9.5 mL, 0.10 mol) dissolved in tetrahydrofuran (10 mL) and stir for 45 minutes. Add m-anisaldehyde (13.6 g, 0.10 mol) in 10 mL tetrahydrofuran, stir for 45 minutes and let warm to room temperature over the weekend. Pour reaction mixture into water, add saturated ammonium chloride (50 mL), separate and dry. Extract with ether (twice), wash combined aqueous layers with saturated sodium chloride, dry, evaporate and purify by flash (silica) chromatography using a graded solvent mixture of dichloromethane to 10% ethyl acetate in dichloromethane to give the title compound as an oil (12.74 g, 51% Yield). NMR agrees with the final, desired compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07253165B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-0b4136e69fa14d5aabb9d73c5cf3a4d0
출처 메모uspto-grants-2007_08