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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1073513생성일: 2026년 10월 24일

2-Chloropyridine → Pyriproxyfen

https://huagongshe.com/ko/reaction/1073513

반응식

참여 물질

역할이름HCID투입량
반응물2-ChloropyridineHCID 7977—
반응물Sodium hydrideHCID 24758—
반응물1-(4-Phenoxyphenoxy)propan-2-olHCID 10399568—
반응물HCID 178418361HCID 178418361—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물PyriproxyfenHCID 9175379%

반응 단계

To a suspension of sodium hydride (200 mg, 5.0 mmol; 60% in oil) in dimethylformamide (5 ml), a solution of 1-methyl-2-(4-phenoxyphenoxy)ethanol (1.22 g, 5.0 mmol) in dimethylformamide (3 ml) was dropwise added with stirring, and the mixture was kept at an inner temperature of 50° to 60° C. until the generation of hydrogen gas ceased. 2-Chloropyridine (684 mg, 6.0 mmol) was dropwise added thereto, followed by stirring at 100° to 110° C. for 5 hours. The reaction mixture was cooled to room temperature, poured into water (100 ml) and extracted with toluene (40 ml) three times. The toluene layer was dried over anhydrous magnesium sulfate, and the solvent was removed by evaporation. The residue was purified by silica gel column chromatography to give 2-[1-methyl-2-(4-phenoxyphenoxy)ethoxy] pyridine (1.27 g) as pale yellow liquid. nD20.5 1.5823. Upon being allowed to stand for a few days, the liquid solidified to give crystals. M.P., 49.7° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04970222
출처 데이터셋uspto-grants-1990_11
ORD IDord-38987a05ccc84a4cbc15b28bb1829721
출처 메모uspto-grants-1990_11