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HRID 70496作成日:2026年10月25日

Hexachloroethane → 5-Chloro-6-methoxypicolinaldehyde

https://huagongshe.com/reaction/70496

反応式

関与物質

役割名称HCID仕込み量
反応物HexachloroethaneHCID 6214—
反応物1-MethylpiperazineHCID 53167—
反応物6-Methoxy-2-pyridinecarboxaldehydeHCID 12325392—
反応物HCID 178418306HCID 178418306—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物5-Chloro-6-methoxypicolinaldehydeHCID 5845284638.7%

反応条件

温度-78 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822503B2
出典データセットuspto-grants-2014_09
ORD IDord-8f8113c61756436d835c99b67bba97c2
出典メモuspto-grants-2014_09