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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 852088Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/852088

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
Edukt2-ChloropyridineHCID 7977—
Edukt3-MethoxybenzaldehydeHCID 11569—
EduktAmmonium ChlorideHCID 25517—
EduktLithium diisopropylamideHCID 2724682—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt2-Chloro-alpha-(3-methoxyphenyl)-3-pyridinemethanolHCID 2014573351%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07253165B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-0b4136e69fa14d5aabb9d73c5cf3a4d0
Quellennotizuspto-grants-2007_08