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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80413생성일: 2026년 10월 23일

2-Ethylhexanol → 2-Ethylhexyl glycidyl ether

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

반응식

참여 물질

역할이름HCID투입량
반응물2-EthylhexanolHCID 7720—
반응물EpichlorohydrinHCID 7835—
반응물1-Chloro-3-(2-ethyl-hexyloxy)-propan-2-olHCID 11816924—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물2-Ethylhexyl glycidyl etherHCID 17162—

반응 조건

온도90 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846598B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-49e819448eb44f669b1a210cab81cc13
출처 메모uspto-grants-2014_09