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HRID 80413作成日:2026年10月23日

2-Ethylhexanol → 2-Ethylhexyl glycidyl ether

https://huagongshe.com/ja/reaction/80413

反応式

関与物質

役割名称HCID仕込み量
反応物2-EthylhexanolHCID 7720—
反応物EpichlorohydrinHCID 7835—
反応物1-Chloro-3-(2-ethyl-hexyloxy)-propan-2-olHCID 11816924—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物2-Ethylhexyl glycidyl etherHCID 17162—

反応条件

温度90 °C

反応手順

To a flame dried, 500 mL round bottomed flask equipped with an addition funnel charged with epichlorohydrin (15.62 g, 0.17 moles), is added 2-ethylhexanol (16.5 g, 0.127 moles) and stannic chloride (0.20 g, 0.001 moles). The reaction is kept under an argon atmosphere and warmed to 90° C. using an oil bath. Epichlorohydrin is dripped into the stirring solution over 60 minutes followed by stirring at 90° C. for 18 hours. The reaction is fitted with a vacuum distillation head and 1-chloro-3-(2-ethyl-hexyloxy)-propan-2-ol is distilled under 0.2 mm Hg. The 1-chloro-3-(2-ethyl-hexyloxy)-propan-2-ol (4.46 g, 0.020 moles) is dissolved in tetrahydrofuran (50 mL) and stirred at room temperature under an argon atmosphere. To the stirring solution is added potassium tert-butoxide (2.52 g, 0.022 moles) and the suspension is stirred at room temperature for 18 hours. The reaction is then evaporated to dryness, residue dissolved in hexanes and washed with water (100 mL). The hexanes phase is separated, dried with Na2SO4, filtered and evaporated to dryness to yield the crude 2-ethylhexyl glycidyl ether, which can be further purified by vacuum distillation.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846598B2
出典データセットuspto-grants-2014_09
ORD IDord-49e819448eb44f669b1a210cab81cc13
出典メモuspto-grants-2014_09