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HRID 2311생성일: 2026년 10월 24일

Ethylene Glycol → 2-[(6-Chloropyrimidin-4-yl)oxy]ethan-1-ol

https://huagongshe.com/ko/reaction/2311

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물Sodium hydrideHCID 24758—
반응물4,6-DichloropyrimidineHCID 70943—
용매TetrahydrofuranHCID 8028—
생성물2-[(6-Chloropyrimidin-4-yl)oxy]ethan-1-olHCID 12564886—

반응 단계

To a mixture of 4,6-dichloropyrimidine (5.0 g), ethylene glycol (100 ml) and tetrahydrofuran (100 ml)is added sodium hydride (60% dispersion-type, 1.34 g) under ice-cooling. The mixture is stirred at the same temperature for two hours, and evaporated to remove the solvent. The residue is extracted with ethyl acetate, and the ethyl acetate extract is dried, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (solvent; chloroform/ethyl acetate=5:1~2:1) to give 2-(6-chloropyrimidin-4-yloxy)ethanol (5.67 g) as an oily product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728706
출처 데이터셋uspto-grants-1998_03
ORD IDord-f570953042144533ac7122491f64e455
출처 메모uspto-grants-1998_03