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HRID 15169作成日:2026年10月27日

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

https://huagongshe.com/reaction/15169

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物Sodium hydrideHCID 24758—
反応物3,4,6-TrichloropyridazineHCID 95123—
反応物Bromo-dichloropyridazineHCID 86614155—
溶媒TetrahydrofuranHCID 8028—
生成物2-[(3,6-Dichloro-4-pyridazinyl)oxy]ethanolHCID 8176354783%

反応条件

温度0 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732460B2
出典データセットuspto-grants-2010_06
ORD IDord-689cf38eecdb401b8d95ebc27ee19dc3
出典メモuspto-grants-2010_06