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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1980617생성일: 2026년 10월 25일

Acetic Acid → 2-Cyclopenten-1-one, 4-hydroxy-3-methyl-2-(2-propen-1-yl)-

https://huagongshe.com/reaction/1980617

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium ChlorideHCID 5234—
반응물Sodium AcetateHCID 517045—
반응물5-Methyl-2-furylallylcarbinolHCID 70478334—
용매WaterHCID 962—
생성물2-Cyclopenten-1-one, 4-hydroxy-3-methyl-2-(2-propen-1-yl)-HCID 11083209.3%

반응 단계

A buffer solution was prepared by dissolving sodium acetate (1.03 g) and MgCl2.6H2O (0.27 g) in water (200 ml) and adjusting the pH value to 6.0 (20° C.) with acetic acid. In a reaction vessel, 5-methyl-2-furylallylcarbinol (5 g) and the entire amount of the buffer solution as prepared above were charged, and the temperature was elevated up to 150° C. in 35 minutes while stirring. The mixture was stirred at the same temperature for 3 hours. After ice-cooling, sodium chloride (50 g) was added, and the mixture was extracted with methyl isobutyl ketone (100 ml) four times. The extract was concentrated at 60° C. under reduced pressure to remove methyl isobutyl ketone, whereby an oily substance (4.6 g) was obtained. The crude product was purified by column chromatography with silica gel (60 g) (developing solvent, ethyl acetate-n-hexane (1:2 by volume)) to obtain 2-allyl-3-methyl-4-hydroxy-2-cyclopentenone (4.0 g). Yield, 80%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04510329
출처 데이터셋uspto-grants-1985_04
ORD IDord-6a1be963fad348f8b53d43fee6b90076
출처 메모uspto-grants-1985_04