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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70496생성일: 2026년 10월 24일

Hexachloroethane → 5-Chloro-6-methoxypicolinaldehyde

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

반응식

참여 물질

역할이름HCID투입량
반응물HexachloroethaneHCID 6214—
반응물1-MethylpiperazineHCID 53167—
반응물6-Methoxy-2-pyridinecarboxaldehydeHCID 12325392—
반응물HCID 178418306HCID 178418306—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물5-Chloro-6-methoxypicolinaldehydeHCID 5845284638.7%

반응 조건

온도-78 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822503B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-8f8113c61756436d835c99b67bba97c2
출처 메모uspto-grants-2014_09