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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128158생성일: 2026년 10월 24일

Iodoethane → Ethyl 4-pentenoate

https://huagongshe.com/ko/reaction/128158

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Potassium HydroxideHCID 14797—
반응물4-Pentenoic acidHCID 61138—
용매EthanolHCID 702—
생성물Ethyl 4-pentenoateHCID 7478665%

반응 단계

4-Pentenoic acid (12.0 g, 0.120 mol) was dissolved in 200 ml of dry EtOH and KOH pellets (7.1 g, 0.126 mol) were added. The mixture was stirred at room temperature until homogeneous. Ethyl iodide (24.3 g, 0.156 mol) was added and the solution was refluxed for 48 hrs. The cooled solution was poured onto H2O (600 ml) and extracted with pentane (200 ml). The organic extract was washed with H2O (2×500 ml) and dried (MgSO4). Solvent removal afforded 10.0 g (65%) of ethyl 4-pentenoate. From the ethyl 4-pentenoate the corresponding epoxy ester, ethyl 4,5-epoxy-pentanoate, is prepared as follows: ethyl 4-pentenoate (9.90 g, 77.3 mmol), and m-chloroperbenzoic acid (18.5 g, 92.8 mmol, 85% assay) were dissolved in 300 ml of CH2Cl2 and stirred for 18 hr in an oil bath at 50° C. The mixture was then filtered, washed with 10% NaHSO3, saturated aqueous NaHCO3 (2X), and H2O (2X) before drying (MgSO4). Concentration under slight vacuum at room temperature followed by distillation (32° C., 0.07 mm) afforded 6.1 g (55%) of the ethyl 4,5-epoxy-pentanoate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04259249
출처 데이터셋uspto-grants-1981_03
ORD IDord-774198835b9d41f28cfecd808cff5b6e
출처 메모uspto-grants-1981_03