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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1029832생성일: 2026년 10월 27일

Ethylene Glycol → 2-Butyl-4-carbethoxy-5-methyl-2,3-dihydrofuran

https://huagongshe.com/reaction/1029832

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물EthanolHCID 702—
반응물2(3H)-FuranoneHCID 140765—
반응물Sodium BisulfateHCID 516919—
반응물3-Acetyl-5-butyloxolan-2-oneHCID 10856172—
촉매p-Toluenesulfonic acidHCID 6101—
촉매Sodium ethoxideHCID 2723922—
용매WaterHCID 962—
용매CyclohexaneHCID 8078—
생성물2-Butyl-4-carbethoxy-5-methyl-2,3-dihydrofuranHCID 1105296963.5%

반응 조건

온도71 °C

반응 단계

A mixture containing 750 grams of 3-acetyl-5-butyl-dihydro-2 (3H)-furanone (4.0 mols), 750 grams of cyclohexane and 8.6 grams of sodium hydrogen sulfate were heated to reflux. To the refluxing mixture were added 250 grams of ethylene glycol (4.0 mols) over a period of 6 hours while the water formed by the reaction was collected in a Dean Stark Trap. An additional 110 grams of ethylene glycol (1.8 mols) was added over 22 hours to replace glycol carried over with the refluxing cyclohexane (azeotropic agent). After 36 hours, an analysis of the reaction mixture showed that the furanone was 95.4 percent converted to a ketal of the formula ##STR21## An aliquot of 94.5 grams of the mixture (0.22 mols) and 30.5 grams of anhydrous ethanol (0.66 mols) and 0.6 grams of p-toluene sulfonic acid were refluxed at 71° C. for 26 hours. The mixture was then neutralized with 0.73 grams of sodium ethoxide followed by stripping on a Rotovap under vacuum to a temperature of 90° C. The residue was water washed, dried on a Rotovap and distilled to provide 29.6 grams of 2-butyl-4-carbethoxy-5-methyl-2,3-dihydrofuran. The amount of recovered material represented a yield of 63.5 percent based on the amount of furanone reacted and a yield of 66.9% based on a 93.0% conversion of the ketal.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05103026
출처 데이터셋uspto-grants-1992_04
ORD IDord-9c09757cc1a34f5da767f36618e7bbf5
출처 메모uspto-grants-1992_04