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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280236생성일: 2026년 10월 24일

Peracetic Acid → 4-(3-Chloropropyl)-2-cyanopyridine

https://huagongshe.com/ko/reaction/280236

반응식

참여 물질

역할이름HCID투입량
반응물Peracetic AcidHCID 6585—
반응물Potassium CyanideHCID 9032—
반응물4-(3-Chloropropyl)pyridineHCID 205442—
반응물4-(3-chloropropyl)-pyridine-N-oxideHCID 12481756—
반응물4-(3-Chloropropyl)-1-methoxypyridinium methyl sulfate saltHCID 23321882—
용매WaterHCID 962—
용매Dimethyl SulfateHCID 6497—
용매Sodium HydroxideHCID 14798—
생성물4-(3-Chloropropyl)-2-cyanopyridineHCID 23321869—

반응 단계

Peracetic acid (40%, 5.0 ml) is added to 4-(3-chloropropyl)pyridine (5.18 g) at such a rate as to keep the reaction temperature at 80°. The mixture is stirred until the temperature falls to 30°. Excess peracid is destroyed with sodium sulfite solution and the solvent is vacuum distilled. The residue is redissolved in methylene chloride (50 ml), filtered and evaporated to yield and crude 4-(3-chloropropyl)-pyridine-N-oxide which is heated to 80° in dimethyl sulfate (4.66 g) for 2 hours. The resulting 4-(3-chloropropyl)-1-methoxypyridinium methyl sulfate salt is dissolved in 10 ml of water, cooled to 0° and reacted with an ice-cold solution of potassium cyanide (6.7 g, 100 mmol) in 20 ml of 0.25N sodium hydroxide solution for 22 hours. The product is extracted with methylene chloride (3×30 ml) and dried over sodium sulfate. The solvent is evaporated and the residue filtered through 45 g of silica gel with ether to yield 4-(3-chloropropyl)-2-cyanopyridine; NMR (CDCl3) 3.56 (t, 2H), 7.40 (d, 1H), 7.57 (s, 1H), 8.60 (d, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04588732
출처 데이터셋uspto-grants-1986_05
ORD IDord-f275d66e8ba6472993cbe40207dc5ab0
출처 메모uspto-grants-1986_05