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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280711생성일: 2026년 10월 25일

Ethyl vinyl ether → 2,5-dimethyl-4-[(1'-ethoxy)ethoxy]-3(2H)-furanone

https://huagongshe.com/reaction/280711

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl vinyl etherHCID 8023—
반응물FuraneolHCID 19309—
반응물Sodium BicarbonateHCID 516892—
촉매Hydrochloric AcidHCID 313—
생성물2,5-dimethyl-4-[(1'-ethoxy)ethoxy]-3(2H)-furanoneHCID 2332127680.8%

반응 단계

To a heterogenous solution of 2,5-dimethyl-4-hydroxy-3-(2H)-furanone (133.0 g, 1.0 mole) and ethyl vinyl ether (144.0 g, 2.0 moles) at 10° C., under N2, is added dropwise, concentrated hydrochloric acid (1.0 g). The temperature rises to 11° C. and the solution becomes homogeneous. It is stirred for 1.5 hours, and then the coolant is removed. Stirring is continued at room temperature for an additional six hours, after which the reaction is quenched by the addition of solid sodium bicarbonate (10 g, 0.12 mole). The reaction mixture is washed with 100 ml water and a second time with 100 ml of 5% NaHCO3. The product is dried over Na2SO4 and distilled to give a 78.9% yield (161.8 g) of 2,5-dimethyl-4-[(1'-ethoxy)ethoxy]-3(2H)-furanone, b.p. 91° C. (0.05 torr), IR (neat, film) 1200, 1625, 1700, 2030, 2978 cm-1 ; 1H NMR (CDCl3) δ1.20 (t, J=8 Hz, 3), 1.32 (d, J=5 Hz, 3), 1.42 (d, J=7 Hz, 3), 2.2 (S, 3), 3.72 (m, 2), 4.48 (q, J=7 Hz, 1), 5.32 (q, J=5 Hz, 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04590284
출처 데이터셋uspto-grants-1986_05
ORD IDord-4dcb7ad850974758914ce18c7de99969
출처 메모uspto-grants-1986_05