돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70530생성일: 2026년 10월 24일

Ethanol → Ethyl 5-chloropyridine-2-carboxylate 1-oxide

https://huagongshe.com/ko/reaction/70530

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물WaterHCID 962—
반응물Sulfuric AcidHCID 1118—
반응물5-Chloro-2-picolinic acidHCID 2762872—
생성물Ethyl 5-chloropyridine-2-carboxylate 1-oxideHCID 67397297—

반응 단계

Concentrated sulfuric acid (4 mL) was added to a solution of 5-chloropyridine-2-carboxylic acid (25.3 g) in ethanol (500 mL) under ice-cooling, and the mixture was stirred under reflux for four hours. The reaction solution was cooled to room temperature and water was added, followed by extraction with chloroform. The organic layer was dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform only→hexane:ethyl acetate=1:1) and the solvent was evaporated under reduced pressure from the fraction containing ethyl 5-chloropyridine-2-carboxylate. Urea peroxide (30.2 g) was added to a solution of the residue in chloroform (300 mL) under ice-cooling. A mixture of trifluoroacetic anhydride (44.7 mL) and chloroform (300 mL) was added dropwise over 30 minutes, and the mixture was stirred while gradually returning to room temperature for two hours. A saturated sodium thiosulfate solution was added dropwise to the reaction solution, followed by extraction with chloroform. The organic layer was dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give ethyl 5-chloropyridine-2-carboxylate 1-oxide as a yellow oil (36.8 g, quant.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822503B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-8b9f3b0a55c040c6a4e792a8075ae462
출처 메모uspto-grants-2014_09