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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15169생성일: 2026년 10월 27일

Ethylene Glycol → 2-[(3,6-Dichloro-4-pyridazinyl)oxy]ethanol

https://huagongshe.com/reaction/15169

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물Sodium hydrideHCID 24758—
반응물3,4,6-TrichloropyridazineHCID 95123—
반응물Bromo-dichloropyridazineHCID 86614155—
용매TetrahydrofuranHCID 8028—
생성물2-[(3,6-Dichloro-4-pyridazinyl)oxy]ethanolHCID 8176354783%

반응 조건

온도0 °C

반응 단계

A solution of ethylene glycol (55 ml) in tetrahydrofuran (200 ml) was treated at around 0° C. (ice bath cooling) with sodium hydride (60% dispersion in oil, 5.9 g) over 40 minutes. After the addition was complete, 3,4,6-trichloropyridazine (27 g) containing isomers of bromo-dichloropyridazine as impurity was added portionwise and washed in with more dry THF (50 ml) and the mixture was stirred at 0° C. for 1 hour and then at room temperature overnight. The mixture was concentrated (to ⅓ volume) then diluted with aqueous sodium bicarbonate solution and extracted with chloroform (5×) and ethyl acetate (3×). The combined organic extracts were washed with water, dried over sodium sulphate and evaporated and the solids filtered off and washed with CHCl3 (×3) and dried in a vacuum oven overnight at 40° C. affording a white solid (25.5 g, 83%), containing some bromo-derivative (10-15%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732460B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-689cf38eecdb401b8d95ebc27ee19dc3
출처 메모uspto-grants-2010_06