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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70496Erstellt: 23. Oktober 2026

Hexachloroethane → 5-Chloro-6-methoxypicolinaldehyde

https://huagongshe.com/de/reaction/70496

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexachloroethaneHCID 6214—
Edukt1-MethylpiperazineHCID 53167—
Edukt6-Methoxy-2-pyridinecarboxaldehydeHCID 12325392—
EduktHCID 178418306HCID 178418306—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Chloro-6-methoxypicolinaldehydeHCID 5845284638,7%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A solution of methylpiperazine (2.31 g) in tetrahydrofuran (20 mL) was cooled to −78° C., and n-butyllithium (2.64 M, 7.55 mL) was added dropwise in an argon gas atmosphere. After stirring at the same temperature for 15 minutes, a solution of 6-methoxypicolinaldehyde (2.5 g) in tetrahydrofuran was added and the mixture was stirred for 30 minutes. t-Butyllithium (1.59 M, 17.1 mL) was added dropwise to the reaction solution, and the mixture was stirred at the same temperature for one hour and at −40° C. for 15 minutes. The reaction solution was cooled again to −78° C. A solution of hexachloroethane (12.9 g) in tetrahydrofuran (20 mL) was slowly added dropwise, and the mixture was stirred at the same temperature for 30 minutes. The reaction solution was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered, after which the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=20:1→10:1) to give 5-chloro-6-methoxypyridine-2-carbaldehyde as a colorless powder (1.21 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822503B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-8f8113c61756436d835c99b67bba97c2
Quellennotizuspto-grants-2014_09