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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 223786생성일: 2026년 10월 24일

Sodium Chloride → 4-Hydroxy-4-methyl-5-(prop-2-en-1-yl)cyclopent-2-en-1-one

https://huagongshe.com/ko/reaction/223786

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Sodium HydroxideHCID 14798—
반응물Magnesium ChlorideHCID 5360315—
반응물PotassiumHCID 5462222—
반응물5-Methyl-2-furylallylcarbinolHCID 70478334—
용매WaterHCID 962—
생성물4-Hydroxy-4-methyl-5-(prop-2-en-1-yl)cyclopent-2-en-1-oneHCID 12879872—

반응 조건

온도100 °C

반응 단계

In a reaction vessel, water (750 ml) was charged, and the temperature was elevated up to 100° C. to reflux. Then, 5-methyl-2-furylallylcarbinol (24 g) and a solution of MgCl2.6H2O (31.5 g) in water (160 ml) were dropwise added thereto in 2.5 hours and 3.5 hours, respectively. During the addition, the pH value of the reaction mixture was maintained at 5.7 to 5.3 by the addition of an aqueous 10% potassium primary phosphate solution and an aqueous 1 N NaOH solution. After about 1.5 hours from the start of the reaction, the pH value stabilized and remained within said range. After completion of the addition of the aqueous MgCl2 solution, the reaction mixture was stirred at pH 5.5 under reflux at 100° C. for an additional 4.5 hours. Then, the reaction mixture was cooled to 40° C. and neutralized with an aqueous 1 N NaOH solution. After addition of sodium chloride (320 g), the mixture was extracted with toluene (250 ml) four times. The extract was dried over anhydrous magnesium sulfate, and toluene was removed therefrom by distillation at 60° C. under reduced pressure to give an oily substance (21.6 g), which was subjected to distillation under reduced pressure to obtain 2-allyl-3-hydroxy-3-methyl-4-cyclopentenone (20.4 g). Yield, 85%. B.P., 88°-90° C./0.5 mmHg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04356326
출처 데이터셋uspto-grants-1982_10
ORD IDord-228a38bc6eaf450d8a335c22cc7b24f6
출처 메모uspto-grants-1982_10