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HRID 852088作成日:2026年10月26日

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

https://huagongshe.com/reaction/852088

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物2-ChloropyridineHCID 7977—
反応物3-MethoxybenzaldehydeHCID 11569—
反応物Ammonium ChlorideHCID 25517—
反応物Lithium diisopropylamideHCID 2724682—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物2-Chloro-alpha-(3-methoxyphenyl)-3-pyridinemethanolHCID 2014573351%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07253165B2
出典データセットuspto-grants-2007_08
ORD IDord-0b4136e69fa14d5aabb9d73c5cf3a4d0
出典メモuspto-grants-2007_08